Life Insurance Jobs in Waltham
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Looking for Life Insurance jobs in Waltham? Browse our curated listings with transparent salary information to find the perfect Life Insurance position in the Waltham area.
Sales Support Coordinator
Company: Buyers Edge Platform
Location: Waltham
Posted Nov 15, 2023
Fresh Concepts, a premier produce procurement company, is seeking a remote Sales Support Coordinator. The role involves administrative duties to boost sales, data management, and support for the sales team and Buyers Edge Platform. The company offers comprehensive benefits, including health insurance, a 401(k) plan, and a supportive work environment. Fresh Concepts, founded in 1987, is committed to fostering diversity and providing equal opportunities.
Scientist I, Analytical Development
Company: Elevatebio
Location: Waltham
Posted Nov 10, 2023
ElevateBio, a technology-driven cell and gene therapy company, is seeking a Scientist, Analytical Development to optimize, transfer, and execute analytical methods for mRNA, oligos, LNPs, and other cell and gene therapy products. The role involves working cross-functionally with various teams and external partners. Requirements include a M.S. or Ph.D. in Biochemistry or related sciences, experience in developing and qualifying assays for mRNA and mRNA-LNP formulations, and understanding of ICH/FDA guidelines. ElevateBio offers cutting-edge technologies and expertise to change the future of medicine.
Director, Biostatistics
Company: Dyne Therapeutics
Location: Waltham
Posted Nov 17, 2023
Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. DSURs, Briefing Documents, etc. This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload. The ideal candidate must be a good communicator, exhibit high-energy, self-motivation, and forward‑thinking. LI-Onsite The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Primary responsibilities include: Serve as a biostatistics expert for assigned clinical studies or compound-level activities Effectively interact with members in other functions including medical, regulatory, safety, clinical operation, and translational medicine for strategic planning to ensure optimized clinical development in accordance with corporate objective Work collaboratively with internal and external (e.g., CRO) team members to coordinate the planning and execution of statistical deliverables Contribute to clinical protocol development, including authoring of the Statistics section and reviewing of other sections by applying statistical principles Design and specify stratification /randomization schema; review and approve test randomization lists Collaborate with Data Management, Clinical Development and Clinical Operations on design and review of eCRFs, and ensure data collection meet the requirements of statistical analyses Author or oversee the development of statistical analysis plans for clinical trials and for integrated summaries of safety/effectiveness (ISS/ISE), provide guidance to statistical programmers on SDTM/ADaM and oversee the development of shells for tables, figures and listings Provide statistical input to data monitoring committee (DMC) charters, independent review charters, and other study-level documents Validate the results of key statistical deliverables Contributes to clinical study reports and other regulatory documents e.g. Perform ad hoc and exploratory statistical analyses as needed Be accountable for assigned statistical activities in support of IND/NDA/MAA or other regulatory submissions Address statistical questions/comments from FDA and other regulatory agencies, and review and address comments by IRB/ECs Support and contribute to the preparation of publications, including manuscripts, posters and oral presentations Represent Dyne regarding statistical issues in meetings with external parties including regulatory agencies and corporate partners Identify and implement emerging new ways of doing clinical development and new methodologies Contribute or lead standardization and process improvement efforts for Biostatistics function and contribute to cross-functional process improvement efforts Education and Skill Requirements: Ph.D. in statistics or Biostatistics or equivalent with at least 8 years of experience in the pharmaceutical or biotech industry Interest in and basic understanding of biology and biological process including ASO and siRNA Demonstrated ability and experience in the design, analysis and reporting of clinical trials Experience in NDAs, MAAs or other regulatory submissions desirable In-depth knowledge of statistical methods for clinical trials, including both frequentist and Bayesian approaches Knowledge of FDA, EMA and ICH regulations and guidelines Proficient in statistical programming (SAS is required and R is a plus) Experience with trial design software (e.g., EAST) Ability to concurrently lead statistical efforts for multiple studies Understanding of data standards, including SDTM and ADaM Adept at overseeing statistical services provided by CRO’s and/or contractors Ability to work independently and act with initiative to address issues Ability to effectively communicate statistical concepts in a clear and concise manner both written and verbally. This person will be responsible for statistical activities including: designing innovative clinical trials, authoring statistical sections of protocols, preparing statistical analysis plans, ensuring quality in implementation of statistical analysis, interpreting and communicating the results of statistical analysis of clinical trial data in support of regulatory submissions as well as manuscripts, and leading biostatistics support for worldwide regulatory submissions. The employee may be requested to perform different or additional duties as assigned.
Scientist- Antibody Development
Company: Abcam
Location: Waltham
Posted Nov 17, 2023
Abcam, a company dedicated to providing tools for scientific research in critical areas like cancer and neurological disorders, is seeking an Antibody Development Scientist. The role involves overseeing the entire antibody development process, from immunization to production, ensuring high-quality RabMabs. The ideal candidate will have a Ph.D. in life sciences, hands-on experience in various assays, and excellent communication skills. Abcam offers competitive benefits, including flexible working hours, generous leave policies, and a focus on employee development.
Senior Corporate Counsel
Company: Evolv Technology
Location: Waltham
Posted Nov 18, 2023
Evolv is seeking a Senior Corporate Counsel to join their Legal Team. The role involves providing legal guidance on strategic initiatives, handling contract negotiations, and managing legal risks. The successful candidate will be seen as a trusted advisor, contribute to the legal strategy, and help develop a comprehensive compliance program. The role is based in Waltham, MA, with the possibility of remote work for the right US-based candidate. The salary range is $174,000-$226,000 + bonus + equity + benefits.
Production Planner
Company: Abcam
Location: Waltham
Posted Nov 17, 2023
Abcam, a company dedicated to providing tools for scientific research in critical areas like cancer and neurological disorders, is seeking a Production Planner. The role involves creating production schedules, adjusting them based on changing conditions, and ensuring they meet customer needs. The ideal candidate should have a degree in a related discipline, experience in manufacturing supply chain planning, and a strong understanding of ERP systems. Abcam offers competitive salaries, flexible benefits, and a supportive work environment that champions diversity and inclusion.
Talent Acquisition Specialist
Company: Buyers Edge Platform
Location: Waltham
Posted Nov 15, 2023
Buyers Edge Platform (BEP) is a technology-enabled group purchasing network that provides group purchasing services, SaaS-based technology solutions, and supply chain consulting and procurement-related services to various foodservice operators. BEP represents over $35 Billion in Network Transactions and is committed to helping foodservice operators thrive by saving them money and improving product quality. The company is seeking a Talent Acquisition Specialist to manage the full life-cycle recruitment process for primarily Sales and Supply Chain positions. The role involves strategic talent sourcing, partnership with business leaders, innovative talent acquisition, recruiting process management, candidate assessment and selection, championing diversity and inclusion, data-driven recruitment, enhancing employer brand, and ensuring a positive candidate experience. The ideal candidate should have a bachelor's degree, 3-5 years of sales recruitment experience, and advanced skills in utilizing an ATS, sourcing tools, and LinkedIn Recruiter. BEP offers comprehensive benefits, including medical, dental, vision, 401(k) with company match, and a flexible work environment.
Scientist, Neuromuscular Research
Company: Dyne Therapeutics
Location: Waltham
Posted Nov 17, 2023
Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. Experience with established molecular techniques including qPCR, western blotting, ELISA, immunohistochemistry/immunofluorescence, fluorescence in-situ hybridization, flow cytometry, and confocal microscopy. Strong written and oral communication skills, organization, and multitasking, and working in a highly collaborative and cross-functional research environment. This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload. Experience in providing scientific and technical leadership applied to novel assay development, advancing challenging drug discovery programs, and mentoring junior colleagues. LI-Onsite The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Contribute to a culture of strong scientific curiosity and build a positive, team-oriented environment. This position may change or assume additional duties at any time. The employee may be requested to perform different or additional duties as assigned.
Senior Research Associate, Platform Development
Company: Dyne Therapeutics
Location: Waltham
Posted Nov 17, 2023
Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload. Perform biochemical analysis on in-process and final purified conjugates including the following techniques: mass spectrometry (MS), CE-SDS, SDS-PAGE, BCA, SEC-HPLC, and UV-vis Perform Tangential Flow Filtration (TFF) Maintain an electronic lab notebook in a timely manner and contribute to company intellectual property Communicate experimental results to a diverse audience of scientific collaborators Serve as functional area representative on cross-functional drug discovery teams Write technical reports to support documentation and technical transfer Contribute to critical discussions of therapeutic structure, function, and new targets Education and Skills Requirements: Minimum of a B.Sc in chemistry, chemical biology, or biochemistry and 4 years of experience in drug discovery and development, preferably at a clinical stage biotechnology company; or M.Sc and 2 years of experience Demonstrated understanding of the general principles of chemistry/biochemistry Demonstrated proficiency in synthesis, purification, and characterization of protein bioconjugates Demonstrated track record of contributions to research including the ability to work independently and troubleshoot experiments Demonstrated ability to collaborate and contribute to an inclusive and high-functioning team Understand published scientific literature outside of his/her immediate area of expertise and apply this understanding to drive innovation Prepared scientific publications or regulatory submission documents LI-Onsite The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Primary Responsibilities Include: Independently plan and execute multistep bioconjugation reactions to deliver protein-oligonucleotide conjugates, including Preparation of activated oligonucleotides and APIs Execution of protein-oligonucleotide conjugations across protein and payload classes up to multi-gram scale Purification of protein conjugates utilizing AKTA FPLC systems with a variety of different chromatography modes (including CHT, HIC, etc.) The employee may be requested to perform different or additional duties as assigned. This role is based in Waltham, MA without the possibility of being a remote role. The successful candidate will work within a group of bioconjugate chemists, biochemists, and analytical scientists, generating and presenting their own data. This position may change or assume additional duties at any time. All Employees are expected to adhere to all company policies and act as a role model for company values.
Sr. Manager of Digital Marketing
Company: Allego
Location: Waltham
Posted Nov 14, 2023
Allego, a rapidly growing SaaS technology company in Boston, is seeking a Senior Manager of Digital Marketing. The role involves crafting digital marketing strategies, enhancing online outreach, and ensuring a seamless digital experience. The ideal candidate should have 5+ years of digital marketing experience, preferably in a B2B SaaS setting, with expertise in Google, LinkedIn, G2, Trustradius, and marketing automation platforms like Hubspot. The candidate should also have a proven track record of designing and executing successful digital campaigns, strong data analytics skills, and excellent communication abilities.
Senior Director of Channel
Company: Evolv Technology
Location: Waltham
Posted Nov 14, 2023
Evolv Technology is seeking a Senior Director of Channel to lead the refinement and execution of their Channel Strategy. The role involves developing and implementing metrics, recruiting new partners, building strong relationships, and driving tangible business outcomes. The ideal candidate should have experience in leading a channel business, creating and developing Channel Strategy and Programs, and building partner programs for software and hardware. The role requires a high level of detail-orientation, the ability to turn strategy into action, and strong leadership skills. The successful candidate will partner internally with various teams to drive scale and ensure success. The role is remote with an expectation to connect with the team in the field approximately 50% of the time. The salary range is $169,000-$271,000 + bonus + equity + benefits.
Associate Director, Statistical Programming
Company: Dyne Therapeutics
Location: Waltham
Posted Nov 17, 2023
Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. Primary Responsibilities Include: Lead and manage the statistical programming activities for clinical trials and studies, ensuring high-quality deliverables and adherence to timelines Collaborate with biostatisticians, data managers, and cross-functional teams to define programming strategies and requirements Develop, validate, and maintain analysis datasets (CDISC standards), tables, listings, and figures, TLFs) in accordance with regulatory guidelines and internal standards Review statistical analysis plans (SAPs) to provide feedback and strategy to the team to execute the plans Perform complex statistical analyses and simulations using SAS, and R, to support clinical trial design and data interpretation Provide expertise in statistical programming for regulatory submissions (e.g., FDA, EMA), including electronic submission standards (eCTD) Build and maintain software agnostic solutions/macros to automate repetitive tasks. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload. Provide novel solutions to the Biometrics and cross-functional teams to better understand the data Mentor and provide guidance to junior programmers, ensuring their growth and development within the team Stay current with industry trends, best practices, and emerging technologies in statistical programming and data analysis Education and Skills Requirements: Bachelor's or advanced degree in statistics, biostatistics, computer science, or a related field Minimum of 8 years of experience in statistical programming within the pharmaceutical or biotech industry Proficiency in SAS and R is essential; experience with Python is desirable Strong knowledge of CDISC standards (SDTM, ADaM) and regulatory requirements for clinical trials Demonstrated leadership and project management skills, including the ability to lead cross-functional teams Excellent communication and interpersonal skills Detail-oriented with a commitment to data accuracy and quality Ability to adapt to changing priorities and manage multiple projects simultaneously LI-Onsite The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. This role assists the Head of Statistical Programming to contribute to departmental strategies and helps to drive the development and continuous improvement of departmental procedures, training, and standards. This position serves as the program team point person for statistical programing and data standards, provide consultation to the program teams, and be responsible for building a statistical programming team to support the Dyne clinical portfolio. For more information, please visit https://www.dyne-tx.com/, and follow us on Twitter, LinkedIn and Facebook. This position may change or assume additional duties at any time. The employee may be requested to perform different or additional duties as assigned.