Contract Jobs in USA
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Looking for Contract jobs in USA? Browse our curated listings with transparent salary information to find the perfect Contract position in the USA area.
Contracts Manager
Company: Sprout Social
Location: USA
Posted Apr 12, 2024
Sprout Social is seeking a Contracts Manager for its Legal team, offering opportunities for growth, collaboration, and a supportive work environment. The role involves negotiating contracts, managing the Legal Service Desk, and overseeing contract management processes. The ideal candidate is a self-starter with strong attention to detail, communication skills, and relevant experience. Benefits include competitive compensation, comprehensive insurance, flexible work arrangements, and opportunities for professional development.
Enterprise Customer Success Manager
Company: Hostaway
Location: USA
Posted Apr 12, 2024
Hostaway, a SaaS startup revolutionizing the vacation rental industry, is seeking an Enterprise Customer Success Manager (CSM) for the North American region. The CSM will ensure customer success and satisfaction by driving platform adoption, upselling, cross-selling, and managing client relationships. Responsibilities include onboarding, problem-solving, ongoing engagement, customer education, collaboration with sales and product teams, and account management. Qualifications include 5+ years of experience in customer success, strong relationship-building skills, problem-solving abilities, excellent communication, and the ability to work independently. The company offers competitive compensation, 100% remote work, equity, values-driven leadership, professional growth opportunities, annual paid leave, and geographic-specific benefits.
Technical Editor I
Company: Trail of Bits
Location: USA
Posted Apr 12, 2024
Trail of Bits is seeking a Technical Editor I to craft compelling technical content, primarily blog posts, that educates and engages the audience on cybersecurity. The role involves developing, editing, and publishing diverse content, overseeing the editing process, ensuring alignment with brand standards, and collaborating with the marketing team. The ideal candidate should have solid experience in technical editing or writing, a meticulous eye for language, quick comprehension of complex subjects, and experience with digital content platforms. The base salary for this full-time position ranges from $80,000 to $110,000, excluding benefits and potential bonuses.
Program Management
Company: R/GA Careers Page
Location: USA
Posted Apr 12, 2024
The text describes the /Associates program, a flexible talent program at R/GA, offering freelance benefits with full-time security and company culture connection. The program is open to former R/GA staff or freelancers with at least three separate bookings or a 12+ week consecutive project. The Program Management team, responsible for project oversight and client relationships, is seeking an experienced Program Manager for a remote role in the US. The ideal candidate should have a track record of developing strong client relationships, managing large teams, and handling multi-million dollar accounts. The hiring range is $2800 to $9500 per week.
Communications Director, Strong Institutions and Infrastructure
Company: Fors Marsh
Location: USA
Posted Apr 12, 2024
Fors Marsh, a certified B Corporation and Top Workplace, is seeking an experienced professional to lead and expand their integrated communications and marketing efforts in the federal non-health sector. The ideal candidate will have 12-15 years of experience in leading new business growth and development for federal agencies, with a strong background in areas such as energy, housing, transportation, and public safety. The role involves strategic planning, new business and proposal development, managing projects, and leading teams. Fors Marsh offers competitive benefits, including top-tier health coverage, remote work, flexible leave, generous retirement contributions, training budgets, and opportunities for volunteering and participating in affinity groups.
Sr Specialist - Contracts
Company: American Specialty Health Incorporated
Location: USA
Posted Apr 12, 2024
American Specialty Health is hiring a Sr Specialist Contracts to support their Legal and Contracts Department. The role involves preparing and managing company and client/vendor template form contracts, serving as a subject matter expert, and collaborating with line of business leadership teams to develop negotiation parameters and strategies. The ideal candidate should have a Bachelor's degree in English, History, Political Science, or equivalent, with a Master's degree in Health Care Administration, Legal degree, or equivalent preferred. Minimum 3 years of proven experience in contract development and document management is required. Proficiency in MS Office and contract management software is necessary. The role is primarily sedentary, with the ability to work remotely and requires a stable internet connection.
Freelance Data Engineer
Company: The Motley Fool
Location: USA
Posted Apr 12, 2024
The Motley Fool is seeking a skilled Freelance Data Engineer for a 6-12 month contract, working 30-40 hours per week. The role involves expanding and optimizing data pipeline architecture, ensuring consistent data quality, and collaborating with various teams. The ideal candidate should have enterprise-level data modeling experience, proficiency in SQL, Python, and AWS services, and experience with Apache Airflow and Snowflake. The company values diversity, inclusion, and equity, and offers a culture of trust, fun, and commitment to making the world smarter, happier, and richer.
Strategic Sourcing Manager - Indirect, IT Software
Company: Workiva
Location: USA
Posted Apr 12, 2024
The job posting is for a Strategic Sourcing Manager position at Workiva, which involves managing long-term agreements, building relationships with stakeholders, and analyzing spending data to identify sourcing initiatives. The role requires a bachelor's degree in a related field and 6 years of experience in strategic sourcing, with a focus on IT projects for software and services.
Lead Mobile App Developer
Company: Nutrafol
Location: USA
Posted Apr 12, 2024
The company is seeking an experienced Lead Flutter Developer to manage mobile app development, collaborate with various teams, and ensure high-quality code. The ideal candidate should have 4+ years of commercial experience in Flutter development, strong technical skills, and a commitment to quality and detail. Preferred qualifications include a degree in Computer Science, experience with Firebase, and a desire to learn new technologies.
Land Acquisition Manager—Community Solar & Storage
Company: Qcells
Location: USA
Posted Apr 12, 2024
The job posting is for a Land Acquisition Manager and Sales Associate to identify and secure land for Community-Scale Solar and Storage projects. The candidate will perform site screening, negotiate contracts, and maintain a log of due diligence payments. The company offers benefits such as medical, dental, and vision insurance, paid time off, and tuition reimbursement.
Vice President, Regulatory Operational Excellence
Company: IMVT Corporation
Location: USA
Posted Apr 12, 2024
<p><strong> <strong><p> <p><strong>Organizational Overview<strong><p> <p>Immunovant is a clinicalstage biopharmaceutical company with a company vision focused on enabling normal lives for patients with autoimmune diseases Our lead asset IMVT1401 is a novel fullyhuman antiFcRn monoclonal antibody in clinical development for multiple indications delivered as a subcutaneous injection for the treatment of autoimmune diseases mediated by pathogenic IgG antibodies Immunovant is committed to developing innovative therapies that not only treat the symptoms but modify the course of autoimmune diseases while restoring hope and health to patients with autoimmune disease by developing and delivering highvalue restorative therapies that enable them to live normal lives<p> <p> <p> <p><strong>The Role<strong><p> <p>This newly created role within the Regulatory Affairs organization is an exciting opportunity for a seasoned Regulatory Affairs professional to serve as a leader in the oversight and optimization of multiple groups within the Regulatory Affairs department The VP of Regulatory Affairs Operational Excellence reports to the Senior Vice President of Regulatory Affairs and will be responsible for overseeing the following Regulatory groups<p> <ul style=> <li style=>Regulatory Operations <ul style=> <li style=>Regulatory Operations is responsible for regulatorysubmission coordination incl development of submission content plans and timelines regulatory information management and regulatory submissions business processes related to submission publishing standards and correspondence archival and Veeva RIM utilization and RIMSMART<li> <ul> <li> <li style=>Regulatory Business Operations <ul style=> <li style=>Regulatory Business Operations is responsible for development of best practices for information sharing and document writing vendor management including regulatory consultants subscriptions and contract medical writers assessment of new technologies to improve efficiency in endtoend regulatory support of clinical development programs and developmentassessment of overall regulatory and medical writing department budgets<li> <ul> <li> <li style=>Medical Writing <ul style=> <li style=>Immunovant Medical Writing is composed of both inhouse and contract writers The team is responsible for development of writing standards and best practices writing of documents including briefing documents clinical protocols CTD modules investigators brochures clinical study reports responses to Health Authority queries etc<li> <ul> <li> <ul> <p>The ideal candidate will have subject matter knowledge in the above Regulatory arenas SHe should have a proven track record of managing multiple functions and people with the discretion to appropriately prioritize initiatives and needs of their teams groups and individuals in a fastpaced and dynamic environment This position will need to have strong relationships across all functions associated with document content writing management and retention requirements This position will drive operational transformation to accommodate near and longterm corporate objectives that require Regulatory operational foresight SHe will review clinicalregulatory documents to support all phases of drug development by leading MW project management activities of an interdisciplinary team to ensure documents are strategic high quality and comply with internal and external standards SHe will delegate workplans for ongoing initiatives as appropriate and provide leadership and strategic support for the team responsible for development and implementation<p> <p> <p> <p><strong>Key Responsibilities <strong><p> <ul style=> <li style=>Manage for 3 to 6 Regulatory personnel including the Senior Director heads of Regulatory Operations and Medical Writing who will also have their own direct reports<li> <li style=>Manage budget for Medical Writing and Regulatory Affairs department<li> <li style=>Manage short term and long term activities and initiatives of Regulatory Operations Regulatory Business Operations and Medical Writing while adapting to changing priorities of the company and overall portfolio of programs<li> <li style=>Development and rollout of document templates and writing standards to ensure compliance with regulations GxP standards and other internalexternal guidelines<li> <li style=>Portfoliolevel oversight to ensure key content messaging messaging in regulatoryclinical documents across 1401 and 1402 programs<li> <li style=>Drive organizational improvement by proactively communicating with Regulatory and crossfunctional stakeholders to problemsolve and identify appropriate operating models for each of the relevant functions<li> <li style=>Serve as a conduit of information flow between Regulatory leadership and the functions overseen by this position Identify opportunities for synergies across the Regulatory organization<li> <li style=>Present various topics and recommendations to Immunovant executive leadership<li> <li style=>Ensure teams are tracking towards timely completion of deliverables<li> <li style=>When necessary serve as intermediary between vendors in support of Immunovant Regulatory staff<li> <li style=>Assess and communicate regulatory requirements to ensure all development activities are in compliance with applicable regulations and guidelines<li> <li style=>Continually evaluate appropriateness and effectiveness of quality standards templates information technology platforms and processes identify opportunities for improvements<li> <li style=>Foster the growth and development and provide mentorship for the Regulatory Affairs team<li> <ul> <p><strong> <strong><p> <p><strong>Requirements<strong><p> <ul style=> <li style=>Bachelors degree in a scientific discipline required advanced degree highly desired<li> <li style=>Minimum 1215 years regulatory industry experience in biopharmaceuticals<li> <li style=>Experience with Veeva and implementation of new processes within Veeva<li> <li style=>Experience with management of a budget to facilitate fiscal planning and accountability of spending<li> <li style=>Handson or oversight experience with regulatory support of clinical trials regulatory operations and submission management and regulatory writing<li> <li style=>Experience with clinical stage assets required experience with BLAMAA and postmarketing strongly preferred<li> <li style=>Highly effective communication skills and confidence to lead strongly when necessaryappropriate<li> <li style=>Ability to pivot comfortably and judiciously communicate change within a rapidly evolving company environment<li> <li style=>Understanding of policy laws regulations and guidelines as they apply to Regulatory Agencies for drug development and approval<li> <li style=>Strong knowledge of eCTD elements and structure with regulatory writing skills<li> <li style=>Strong knowledge of drug development FDA EMA and other guidelines and regulations<li> <li style=>Working knowledge of electronic submission procedures and document management system requirements<li> <li style=>Working knowledge of regulatory submission management electronic publishing and document management Experience with Veeva systems strongly preferred<li> <li style=>Experience of filing NDABLAMAA application and meeting submission quality and standards<li> <li style=>Demonstrated experience with effective management of direct reports contractorsconsultants and vendors<li> <ul> <p> <p> <p><strong>Work Environment<strong><p> <ul style=> <li style=>Dynamic interactive fastpaced and entrepreneurial environment<li> <li style=>Immunovants headquarters is located in New York City The position will be remote work<li> <li style=>Domestic travel required up to 20<li> <ul> <p> <p> <p>Compensation is based on a number of factors including market location and may vary depending on jobrelated knowledge skills and experience Equity signon bonuses and other forms of compensation may be provided as part of a total compensation package in addition to a full range of medical dental vision 401k and other benefits including unlimited paid time off and parental leave The annual base salary for this position ranges from $32000000 $34000000<p> <p> <p> <p> <p><img src=httpsremotivecomjobtrack1906512blankgifsource=publicapi alt=>
Data Visualization Specialist
Company: The Motley Fool
Location: USA
Posted Apr 12, 2024
The Motley Fool is seeking a skilled Data Visualization Specialist with ThoughtSpot experience for a 6-month contract. The role involves creating and optimizing ThoughtSpot solutions, collaborating with various teams, and ensuring data accuracy and consistency. The ideal candidate should have 2+ years of ThoughtSpot experience, strong data visualization skills, intermediate SQL skills, and proficiency in Snowflake. Excellent communication and problem-solving abilities are also required.