Travel Jobs in Cambridge, MA
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Senior Executive Business Partner to CMO
Company: Klaviyo
Location: Boston, MA
Posted Aug 08, 2023
We do not discriminate on the basis of race, ethnicity, citizenship, national origin, color, religion or religious creed, age, sex (including pregnancy), gender identity, sexual orientation, physical or mental disability, veteran or active military status, marital status, criminal record, genetics, retaliation, sexual harassment or any other characteristic protected by applicable law.You can find our Job Applicant Privacy Notice here. If you’re ready to do the best work of your career, where you’ll be welcomed as your whole self from day one and supported with generous benefits, we hope you’ll join us.Upon request, you can receive additional information about the compensation and benefits for this role. Requests can be submitted here. To reach our goals, we need our own crew of remarkable creators—ambitious and collaborative teammates who stay focused on our north star: delighting our customers. Additional information regarding benefits can be found at klaviyorewards.com.Klaviyo is committed to a policy of equal opportunity and non-discrimination. We see limitless potential for the technology we’re developing to nurture personalized experiences in ecommerce and beyond. This is a great opportunity for a self-motivated, organized, and eager project manager to work directly with members of our leadership team. Support in the C-level is preferred.You have experience supporting C-level executives (highly preferred).You have experience booking travel and completing expense reports and maybe have experience holding your own corporate card (preferred).You have experience with managing Board of Directors related activities and high profile events such as managing event logistics, especially in a project manager capacity.You’re highly adept in Google Suite, Slack, Zoom, and other communication technologies.You are intellectually curious and maintain a high level of confidentiality.You are proactive in anticipating the needs of the people you support and in obtaining the information you need to execute your projects.You have a team-first mentality and have experience collaborating with key stakeholders on multiple projects.You are able to work independently and are a self-starter.You are on a journey of continuous improvement, and you proactively seek and implement constructive feedback to level up your skills and knowledgeYou possess excellent verbal and written communication skills, ability to influence, and exceptional organizational skills and attention to detail.LI-OnsiteGet to Know KlaviyoWe’re Klaviyo (pronounced clay-vee-oh). In this role you will:Oversee scheduling and calendar management for assigned executives, including working with executives to prioritize their time and attendance.Provide strategic input on executive level project managementManage the operational cadence of the organization you support to ensure that all pre-planning, meeting scheduling, and follow-ups are completed for major business initiatives throughout the year.Be the second set of eyes on all major business initiative planning and communication to ensure efficient allocation of resources and effective communication for cross-functional collaborations.Attend meetings, take notes on action items, and follow up with content and deliverables as needed.Manage logistics for quarterly executive off-sites and other meetings and events as needed.Help set agendas and review content for leadership meetingsComplete travel arrangements and expense reports for the executives you support.Take ownership of small projects as they come up for example, crafting team communications, managing overall budget and plan events for the team within the budget requirements Willing to go above and beyond to manage changing calendar commitments and seamless global travel schedulingAbility to travel - 20% travel may be required for this roleWho You Are:You have 6 years experience in an administrative support role. Executive Business Partners at Klaviyo have insight into the vision and strategy of a leading tech company in hyper-growth mode while having hands-on impact on executing that vision.How You Will Make a Difference:A successful Executive Business Partner at Klaviyo will be a methodical, organized, take-charge project manager and executive support coordinator who has a deep understanding of all of Klaviyo’s business needs and the impact of major initiatives across departments.
Director, GMP Quality Assurance
Company: Entrada Therapeutics
Location: Boston, MA
Posted Aug 07, 2023
Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.Third Party Staffing AgenciesEntrada does not accept unsolicited resumes from any source other than directly from candidates. The successful candidate will have a strong understanding of GMP Quality for raw materials, drug substance, drug product, and label and packaging, including QC testing, stability, and distribution. We value work life balance, you'll benefit from discretionary time off, paternity leave, and an excellent 401(k) package. The position will focus initially on GMP Quality build-out to strengthen Clinical-phase Quality Systems, ensuring that systems and processes developed will accommodate global Quality System requirements. The position is based in Boston, MA and reports directly to the Sr. Director, Quality Assurance.ResponsibilitiesLead QA oversight of GMP activities at Entrada and its contract development and manufacturing organizations (CDMOs), testing laboratories, and logistics vendors.Develop and implement risk-based Quality strategies for investigational and materials including establishment and maintenance of phase appropriate quality systems; proactively identify and mitigate quality risks.Be responsible for quality-related activities and requirements to enable release of Raw Materials, Drug Substance, Drug Product, and Finished Goods.Oversee GMP/GDP vendor management, assuring that vendors are operating in compliance with the applicable quality program and regulations/ guidelines and are prepared for Regulatory inspections.Lead development, implementation, and maintenance of GMP Quality Systems and SOPs related to GMP/GDP activities.Lead Quality investigations, including input and approval of plans for resolution of product-impacting Quality issues; provide oversight of appropriate CAPAs associated with investigations, deviations, product complaints and recalls.Provide quality input and oversight for process validation, process performance qualification, and continuous process verification.Oversee clinical distribution, logistics, and launch activities.Collaborate with CMC to establish metrics and report the state of GMP Quality and compliance of GMP vendors to senior management.Ensure CMC and GMP/GDP vendor activities are compliant with cGMP, FDA, ICH, EMA regulations and guidelines and industry standards.Stay abreast of industry developments – forthcoming regulations, guidance, best practices, and etc., training and mentoring staff on global GMP regulations and guidance.Ensure external inspection readiness and pre-approval Regulatory inspection readiness to prepare for audits by external parties and global Regulatory Health Authorities.The NecessitiesAt Entrada, our passion for science, our devotion to patients and our values drive our behavior:Humanity - We genuinely care about patients and about one another.Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients.Creativity - We are creative problem solvers.Collaboration - We are more than the sum of our parts.Curiosity - We have a growth mindset and push conventional thought and theory.To thrive on our team, you will need to come with:Minimum BS degree in Science or Engineering, advanced degree a plus, and 10 years of applicable pharmaceutical drug development experience with at least 8 years of Quality Assurance experience, including Supply Chain QA. Useful background could include experience with oligonucleotides, large molecules, parenteral aseptic fills and filing of an IND/NDA.Demonstrated success leading and motivating cross-functional teams and managing direct reports.Track record of delivering in a biotech start-up, fast-paced, innovative, dynamic environment while remaining flexible, proactive, resourceful, and efficient.Direct experience in successfully managing Health Authority Inspections and multiple projects and responsibilities concurrently.Strong working knowledge of global GXP requirements, regulations, and guidance; sound judgment and commitment to ethical conduct.Excellent leadership skills including an effective written and oral communicator, including experience preparing and making presentations to executive level management and interacting effectively with internal and external organizations, collaborators, and customers.Willingness to travel up to approximately 25%.The PerksBy becoming a team member here at Entrada, you’ll have access to competitive health, dental, and vision coverage, as well as life insurance, and short term and long-term disability insurance. The Director, GMP Quality Assurance is accountable for ensuring that vendors are compliant with global regulations, prepared for potential Sponsor and Regulatory Inspections and that the appropriate processes, systems and activities are in place and performed to protect patient safety, product quality, and data integrity.This is an exciting, interdisciplinary role for a highly qualified and motivated individual. The scope of this leadership role includes oversight of GMP activities at Entrada and its contract development and manufacturing organizations (CMOs), suppliers, testing laboratories, and logistics vendors. This expertise, along with drug development background and the organizational and interpersonal skills required to build and foster strong relationships with collaborators, will be needed for success. You excel at building relationships and trust with your key stakeholders.The OpportunityThe Director of GMP Quality Assurance will be responsible for strategic and operational management of manufacturing, testing laboratory, and release and distribution-related Quality activities. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. You are able to lead teams and develop strategies while not being afraid to roll up your sleeves and perform Batch Release, review and approve Analytical Methods, manage CMO quality documentation and write Quality Plans as needed.You are an excellent team player and relationship builder.
Lead Data Scientist
Company: Analog Devices
Location: Boston, MA
Posted Aug 06, 2023
We foster a culture where everyone has an opportunity to succeed regardless of their race, color, religion, age, ancestry, national origin, social or ethnic origin, sex, sexual orientation, gender, gender identity, gender expression, marital status, pregnancy, parental status, disability, medical condition, genetic information, military or veteran status, union membership, and political affiliation, or any other legally protected group. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. As such, applicants for this position - except US Citizens, US Permanent Residents, and protected individuals as defined by 8 U.S.C. Analog Devices, Inc. is an Equal Opportunity Employer. Job Req Type: Experienced Required Travel: Yes, 10% of the time Shift Type: 1st Shift/Days To apply, please submit your resume, a cover letter highlighting your relevant experience, and any supporting documentation or links to relevant projects. Analog Devices is an equal opportunity employer. For positions requiring access to technical data, Analog Devices, Inc. may have to obtain export licensing approval from the U.S. Department of Commerce - Bureau of Industry and Security and/or the U.S. Department of State - Directorate of Defense Trade Controls. Responsibilities: Develop, validate, and implement AI solutions, with a focus on LLMs, to improve our software solutions and capabilities.Analyze complex datasets to extract insights, identify trends, and make recommendations for product enhancements.Collaborate with engineering and software teams to integrate AI models into our software products.Lead data collection efforts to train and refine our AI models.Implement tools and processes to monitor the performance and accuracy of our AI models.Communicate complex data findings and AI concepts to non-technical stakeholders in clear, understandable language.Stay abreast of the latest developments in AI, LLMs, and data science, and integrate these advancements into our work.Mentor junior team members and create a positive, collaborative team environment. EEO is the Law: Notice of Applicant Rights Under the Law.
Account Manager, LC/MS
Company: Agilent Technologies
Location: Boston, MA
Posted Aug 05, 2023
All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility. All individuals, regardless of personal characteristics, are encouraged to apply. Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email [email protected] or contact +1-262-754-5030. Qualifications Bachelors or Masters Degree or University Degree or equivalentTypically 2+ years relevant experience for entry to this levelFamiliarity with liquid chromatography, mass spectrometry, and other analytical chemistryTechnical sales experience is a plus LI-RK1 Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. The ideal candidate will reside in the Boston, MA city limits. Option to Work Remote Yes Travel Required 50% of the Time Schedule Schedule:Full time Shift Day Duration No End Date Job Function Sales In this role, you will be: Responsible for selling of company, systems and services to end-user customers in assigned Boston area territory, pharma and bio-pharma accounts.Responsible for developing customers and their satisfaction.Represents the company to the customer and the customer to the company in all sales-oriented activities.Interprets customer needs and works to meet those needs.Identifies potential business opportunities, able to handle complex leads independently.Works on sales assignments with broadly defined objectives.Solves non-routine issues, challenges and problems within field of specialization. We value diversity at all levels.
Biosciences Account Manager - Sales - Boston
Company: Thermo Fisher Scientific
Location: Boston, MA
Posted Aug 08, 2023
http://jobs.thermofisher.com Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. Personal Attributes Self-motivatedAccountableEffective communicator Location Remote, field-based. MS Office) Competencies Innovative, customer-focused, and growth driven! Join us and chip into our singular mission-enabling our customers to make the world healthier, cleaner, and safer. Boston and CambridgeMinimal overnight travel required At Thermo Fisher Scientific, each one of our 100,000 outstanding minds has a unique story to tell. How will you make an impact In this role, you will directly impact our mission of making the world healthier, cleaner, and safer by providing our life science technologies to Academic, Healthcare, and Biotech customers for use in their life sciences research including cell biology, protein biology, molecular biology, and more. Additional Attributes: Self-Motivation (takes initiative)Self-AwarenessProblem-SolvingPersistentCurious Standout ColleagueListenerOutspoken/ConfidentDetailedPositive can-do demeanorCoachableDrivenStrategic Location/Division-Specific Information Biosciences Division, Life Science Solutions Group - Field-based, BioSciences Account Manager, Academia and Biotech. Apply today! Boston and Cambridge.
ADI Garage Leader
Company: Analog Devices
Location: Boston, MA
Posted Aug 07, 2023
We foster a culture where everyone has an opportunity to succeed regardless of their race, color, religion, age, ancestry, national origin, social or ethnic origin, sex, sexual orientation, gender, gender identity, gender expression, marital status, pregnancy, parental status, disability, medical condition, genetic information, military or veteran status, union membership, and political affiliation, or any other legally protected group. As such, applicants for this position - except US Citizens, US Permanent Residents, and protected individuals as defined by 8 U.S.C. Job Req Type: Experienced Required Travel: Yes, 10% of the time Shift Type: 1st Shift/Days Analog Devices is an equal opportunity employer. The Garage is a fast-paced, high-energy environment located in downtown Boston. For positions requiring access to technical data, Analog Devices, Inc. may have to obtain export licensing approval from the U.S. Department of Commerce - Bureau of Industry and Security and/or the U.S. Department of State - Directorate of Defense Trade Controls. EEO is the Law: Notice of Applicant Rights Under the Law. Requirements A proven track record of building solid relationships with internal stakeholders and customers, understanding their business, pain points, and future directions.Experience collaborating with and influencing cross-functional teams across the enterprise.Broad knowledge of current technologies and future trends.An entrepreneurial mindset with a thirst to explore and monetize the art of the possible.Excellent communication, negotiation and presentation skills.Strong analytical, critical thinking and problem-solving skills.Ability to excel in high-pressure situations. 1324b(a)(3) - may have to go through an export licensing review process. The ideal candidate is a creative thinker with strong leadership and technical skills who has experience in strategic technology creation, ideally in semiconductor or associated industries.
Executive Assistant To The CEO
Company: Linus Health
Location: Boston, MA
Posted Aug 05, 2023
All qualified candidates will receive consideration for employment without regard to race, religion, color, national origin, sexual orientation, gender, gender identity or expression, age, genetic information, disability or any characteristic protected by law. The final offer determined for the candidate hired into this position will depend on a number of factors, including, but not limited to, the candidate's relevant skills, professional experience, labor market conditions, etc.Linus Health is an equal opportunity employer. If you are in need of assistance due to a disability, please contact us. Report problems to the CEO when they cannot resolveSuccessfully completed critical aspects of deliverables with a hands-on-approach, including drafting personal correspondence, emails, and other tasks that facilitate the CEIO' ability to effectively lead the companyPrioritize conflicting meetingsAct as the liaison for CEO between C-Suite and Senior ManagementMaintain discretion and confidentially in relationshipsAbout You:10+ years in a similar EA type role supporting "C level executivesHealthcare, Biotech, Pharma and/or digital health experienceAbility to inspire trust and loyalty given the amount of exposure to confidential informationConfidence in ability to act as a Gatekeeper on behalf of the CEO - proven ability to deter others who want direct access to CEO but perhaps the topic should be resolved by someone elseAbility to pivot and adapt to changing circumstancesProblem solving ability and organizational skillsExcellent platform presentation skills, interpersonal skills, as well as excellent written and verbal communication skills. Provides "gatekeeper" and "gateway” role, creating win-win situations for direct access to the CEO's time. Triage the barrage of information, challenges and background noise that the CEO is bombarded with (this will take time).Anticipates the needs of the CEO and strives to provide services or products before being requestedProvides a bridge for smooth communication between the CEO's office and internal departments, demonstrating leadership to maintain credibility, trust and support the senior management staffWorks closely and effectively with the CEO to keep him well informed of upcoming commitments and responsibilities(both personal and professional), following up appropriately. Acts as a "barometer," having a sense for the issues taking place in the environment and keeping the CEO updated.Interacts professionally with EA's of other high level executives in other organizationsPrep for BOD meetings - once agenda is agreed upon, liaise with legal to prepare consent(s), solicit appropriate content from internal stakeholders for final review by CEO/COO/Legal.Create BOD book for distribution prior to meetingPrepare reports, collect and analyze information, prepare presentationsInteract with customers/partners/vendors when appropriate and problem solveDocument complaints and develop a course of action. Please note that given the nature of the role & our CEO as well as a number of other team members being based in Boston, this person will be required to be in the office 2-3 days a week.What You'll Do:Completes a broad variety of professional and personal operational tasks for the CEO including managing an extremely active calendar of appointments; composing and preparing correspondence that are oftentimes confidential (eventually, after trust is built, responds on behalf of the executive); answers calls, arranges travel plans, itineraries, and agendas.Plans, coordinates and ensures the CEO's schedule is followed and respected. Politically savvy and an excellent communicatorResults driven, detail oriented and demonstrated accountabilityAbility to work as part of a team and independentlyAbility to think strategically9one step ahead of the CEO) yet execute tacticallyGo-getter and results-driven attitude - a self-started with a lot of fire and grit What We Offer:As a health and wellness company, an opportunity to have a lasting impact on the way people and communities engage with brain and mental health, and even to affect the prognoses of people’s mental and brain health trajectoryA mission-driven environment where all 90+ employees strive to exemplify our core values every dayUnlimited PTO -- We know this can work both ways, however our leadership team does an excellent job at encouraging people to take PTOA sincere and deep appreciation for the importance of mental health: We have recently implemented a “monthly flex day” where employees are encouraged to take time away from work to rest, recharge & reset.A peer-to-peer recognition program: Celebrating our employees’ hard work and success is in our DNA!Employee Referral Incentive programA robust healthcare package that includes medical, dental & vision benefits as well as a 401(k) program where Linus will match up to 6% of employee contributionsThe base salary budgeted for this position is in the $90,000-$135,000 range per year. Additionally, you will be the first point of contact for everything that goes through the CEOs office. The role will include an annual discretionary target bonus based on performance as well as equity.
Director, GMP Quality Assurance
Company: Entrada Therapeutics
Location: Boston, MA
Posted Aug 07, 2023
Entrada Therapeutics is a tight-knit team of experts in therapeutic development and rare diseases, aiming to transform the treatment of devastating diseases by establishing a new class of medicines. The company is seeking a highly qualified and motivated individual for the Director of GMP Quality Assurance role, responsible for strategic and operational management of manufacturing, testing laboratory, and release and distribution-related Quality activities.
Full Stack Engineer
Company: Analog Devices
Location: Boston, MA
Posted Aug 07, 2023
We foster a culture where everyone has an opportunity to succeed regardless of their race, color, religion, age, ancestry, national origin, social or ethnic origin, sex, sexual orientation, gender, gender identity, gender expression, marital status, pregnancy, parental status, disability, medical condition, genetic information, military or veteran status, union membership, and political affiliation, or any other legally protected group. )Experience with cloud platforms such as GCP (preferred), AWS, or AzureExperience with Agile/Scrum development processes and tools (e.g., Jira, Confluence, etc. As such, applicants for this position - except US Citizens, US Permanent Residents, and protected individuals as defined by 8 U.S.C. Responsibilities: Design and implement back and front-end components and servicesDesign, implement, and maintain well-abstracted and documented REST APIsCollaborate with other teams to deploy and serve AI/ML models via APIsWork closely with DevOps team to improve system availability, scalability, and reliabilityWork closely with MLOps team to implement, test, and support data pipelines and dataGuarantee product and code quality utilizing best practices such as unit testing, code reviews, etc.Stay up to date with the latest developments in web and data technologies and frameworks Qualifications: 3+ years of experience designing, building, and maintaining distributed web applications and servicesExperience with microservices architectures and REST API development (e.g., FastAPI)Experience with front-end libraries and frameworks such as ReactJS and NextJSExperience with SQL and NoSQL database technologies (e.g., MySQL, MongoDB, etc. Analog Devices transforms physical phenomena - sound, light, radio waves, voltages, currents, and motion - into high-fidelity data. Analog Devices is an equal opportunity employer. For positions requiring access to technical data, Analog Devices, Inc. may have to obtain export licensing approval from the U.S. Department of Commerce - Bureau of Industry and Security and/or the U.S. Department of State - Directorate of Defense Trade Controls. The AI Solutions BU collaborates with our Market BUs to solve problems beyond the reach of pure semiconductor, circuit-level, or architectural innovation. Our mission is to build the Intelligent Edge, where AI transforms how we solve challenging problems by combining deep application knowledge, close customer relationships, extraordinary data, advanced circuits, and breakthrough algorithms. 1324b(a)(3) - may have to go through an export licensing review process.
Biotech Sales Rep - Boston
Company: Avantor
Location: Boston, MA
Posted Aug 05, 2023
We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. For more information about equal employment opportunity protections, please view the Equal Employment Opportunity is THE LAW Poster, EEO is the Law Poster Supplement, and Pay Transparency Non-Discrimination Provision. Work is mostly sedentary but does require walking, standing, bending, reaching, lifting or carrying objects that typically weigh less than 10 lbs. 3rd Party Non-Solicitation Policy: By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor is proud to be an equal opportunity employer. Minimal physical effort is required. EEO Statement: We are an Equal Employment/Affirmative Action employer. Requests for accommodation will be considered on a case-by-case basis. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. If you need a reasonable accommodation for any part of the employment process, please contact us by email at [email protected] and let us know the nature of your request and your contact information.
Scientist/Senior Scientist, Translational Research (Pharmacological Sciences)
Company: Voyager Therapeutics
Location: Cambridge
Posted Aug 08, 2023
This is a primarily on-site role with frequent travel to study sites (10-15%).ResponsibilitiesContribute to experimental design, execution, and data analysis for preclinical studies that support Voyager’s capsid engineering platform and therapeutic programs.Serve as a study monitor to review study protocols and address requests/questions from external collaborators and CROsCoordinate with capsid discover team, therapeutic program leads, and operations to set up studies aligned with project requirements and timelines.Monitor study progress and coordinate study activities, such as shipping and receiving of test article and tissue samplesTravel and monitor in-life studies at CRO sites and report site-visit results to Voyager teamsMaintain and update key events in study log and database and timely communicate study status to program teamsReview study report, perform data analysis, and present study results as needed RequirementsAn advanced scientific degree (DVM / PhD) degree in Pharmacology, Biology, or a relevant discipline, with a minimum of 2 years of relevant experience OR a Master’s degree with 5+ years of experience OR a Bachelor’s degree with 8+ years of experienceExperience working with animals is requiredFamiliarity with in vivo techniques, preferably hands-on experience Competency with database, spreadsheet, and presentation applications (e.g., Excel, PowerPoint, Smartsheet, Data entry systems, or similar)Skilled in data analysis using statistical software such as GraphPad Prism, JMP, etc.Outstanding problem-solving skills and ability to multi-task is required.Experience with pharmacology / toxicology study protocol generation, study design, and writing / editing study reports Self-motivated, able to work independently and with team members, highly organized with strong attention to details, and willingness to travel to CRO sitesPreferred qualifications / experienceManagement and / or execution of animal studies at a CRO environment is a plusUnderstanding of relevant biostatistical principles for analysis of animal study dataFamiliarity with bioanalytical and molecular biological techniquesFamiliarity with clinical trials for biologics developmentPrior experience in neuroscience and knowledge of neuroanatomy This is an ideal position for a candidate with a strong background and hands-on experience in preclinical studies, who thrives in a team-oriented, fast-paced, and cross-disciplinary start-up biotech environment.The candidate will contribute to the design and execution of various pharmacology and toxicology studies to support development of novel capsids and biotherapeutics such as AAV-based gene therapy. The Scientist will interact with cross-functional capsid discovery and research program teams to execute in vivo pharmacology, biodistribution, PK/PD, and toxicology studies using AAV-based gene therapy approaches. The successful candidate will work with our multidisciplinary team in Cambridge, Massachusetts. Voyager’s pipeline includes preclinical programs in Parkinson’s disease, Alzheimer’s disease, and amyotrophic lateral sclerosis (ALS), each with validated targets and biomarkers to enable a path to rapid potential proof-of-biology. The candidate will also perform quality control and analyze study data and communicate study progress through presentations and written reports. This platform is fueling alliances with Pfizer Inc., Novartis and Neurocrine Biosciences as well as multiple programs in Voyager’s own pipeline. For more information, visit www.voyagertherapeutics.comJob SummaryVoyager Therapeutics is growing and seeking an experienced and highly motivated Scientist/Senior Scientist to join our Pharmacological Sciences team who shares our passion for the promise of gene therapy. Voyager’s TRACER AAV capsid discovery platform has generated novel capsids with high target delivery and blood-brain barrier penetration at low doses, potentially addressing the narrow therapeutic window associated with conventional gene therapy delivery vectors. The potential of both disciplines has been constrained by delivery challenges; Voyager is leveraging innovative expertise in capsid discovery and deep neuropharmacology capabilities to address these constraints. About VoyagerVoyager Therapeutics (Nasdaq: VYGR) is a biotechnology company dedicated to breaking through barriers in gene therapy and neurology.
Scientist/Senior Scientist, Translational Research (Pharmacological Sciences)
Company: Voyager Therapeutics
Location: Cambridge
Posted Aug 08, 2023
This is a primarily on-site role with frequent travel to study sites (10-15%).ResponsibilitiesContribute to experimental design, execution, and data analysis for preclinical studies that support Voyager’s capsid engineering platform and therapeutic programs.Serve as a study monitor to review study protocols and address requests/questions from external collaborators and CROsCoordinate with capsid discover team, therapeutic program leads, and operations to set up studies aligned with project requirements and timelines.Monitor study progress and coordinate study activities, such as shipping and receiving of test article and tissue samplesTravel and monitor in-life studies at CRO sites and report site-visit results to Voyager teamsMaintain and update key events in study log and database and timely communicate study status to program teamsReview study report, perform data analysis, and present study results as needed RequirementsAn advanced scientific degree (DVM / PhD) degree in Pharmacology, Biology, or a relevant discipline, with a minimum of 2 years of relevant experience OR a Master’s degree with 5+ years of experience OR a Bachelor’s degree with 8+ years of experienceExperience working with animals is requiredFamiliarity with in vivo techniques, preferably hands-on experience Competency with database, spreadsheet, and presentation applications (e.g., Excel, PowerPoint, Smartsheet, Data entry systems, or similar)Skilled in data analysis using statistical software such as GraphPad Prism, JMP, etc.Outstanding problem-solving skills and ability to multi-task is required.Experience with pharmacology / toxicology study protocol generation, study design, and writing / editing study reports Self-motivated, able to work independently and with team members, highly organized with strong attention to details, and willingness to travel to CRO sitesPreferred qualifications / experienceManagement and / or execution of animal studies at a CRO environment is a plusUnderstanding of relevant biostatistical principles for analysis of animal study dataFamiliarity with bioanalytical and molecular biological techniquesFamiliarity with clinical trials for biologics developmentPrior experience in neuroscience and knowledge of neuroanatomy For more information, visit www.voyagertherapeutics.com.Voyager Therapeutics® is a registered trademark, and TRACER™ is a trademark, of Voyager Therapeutics, Inc.Job SummaryVoyager Therapeutics is growing and seeking an experienced and highly motivated Scientist/Senior Scientist to join our Pharmacological Sciences team who shares our passion for the promise of gene therapy. This platform is fueling alliances with Pfizer Inc., Novartis Pharma AG, Neurocrine Biosciences, Inc., and Sangamo Therapeutics, Inc., as well as multiple programs in Voyager’s own pipeline. This is an ideal position for a candidate with a strong background and hands-on experience in preclinical studies, who thrives in a team-oriented, fast-paced, and cross-disciplinary start-up biotech environment.The candidate will contribute to the design and execution of various pharmacology and toxicology studies to support development of novel capsids and biotherapeutics such as AAV-based gene therapy. The Scientist will interact with cross-functional capsid discovery and research program teams to execute in vivo pharmacology, biodistribution, PK/PD, and toxicology studies using AAV-based gene therapy approaches. The successful candidate will work with our multidisciplinary team in Cambridge, Massachusetts. Voyager’s pipeline includes wholly owned and collaborative preclinical programs in Alzheimer’s disease, amyotrophic lateral sclerosis (ALS), Parkinson’s disease, and other diseases of the central nervous system, with a focus on validated targets and biomarkers to enable a path to rapid potential proof-of-biology. The candidate will also perform quality control and analyze study data and communicate study progress through presentations and written reports. Voyager’s TRACER™ AAV capsid discovery platform has generated novel capsids with high target delivery and blood-brain barrier penetration at low doses, potentially addressing the narrow therapeutic window associated with conventional gene therapy delivery vectors. About&8239;Voyager Therapeutics Voyager Therapeutics (Nasdaq: VYGR) is a biotechnology company dedicated to breaking through barriers in gene therapy and neurology. The potential of both disciplines has been constrained by delivery challenges; Voyager is leveraging cutting-edge expertise in capsid discovery and deep neuropharmacology capabilities to address these constraints.