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Featured Companies are employers who have come directly to FlexJobs, been approved by our staff, and have directly posted their jobs to the FlexJobs site.
- 100% Remote Work
- Full-Time
- Employee
- 144,000 - 198,000 USD Annually
- US National
Author toxicological risk assessments of both API and drug formulation impurities/degradants as well as evaluation of container closure system extractables and leachables.
- Hybrid Remote Work
- Full-Time
- Employee
- 120,000 - 165,000 USD Annually
- Round Lake, IL
Leads cross-functional teams in defining program strategies, planning, defining scope, execution, developing goals, monitoring and program closure. Accountable for core team performance, project schedule and execution...
- 100% Remote Work
- Full-Time
- Employee
- 142,500 - 237,500 USD Annually
- US National
Lead data-driven feasibility process, develop enrollment forecasts, identify and resolve operational risks, collaborate with stakeholders to inform decision making. Minimum 5 years' experience in pharmaceutical/CRO/biotech industry required.
- 100% Remote Work
- Full-Time
- Employee
- South Korea
Participate in the management and preparation of country submissions. Provide local regulatory strategy advice to internal clients. Coordinate with internal departments for site start-up activities and ensure alignment with submission activities.
- Hybrid Remote Work
- Full-Time
- Employee
- 114,375 - 190,625 USD Annually
- Princeton, NJ
Establish global clinical trial supply strategy, advise clinical team on resource constraints, improve efficiency of clinical supply processes, ensure compliance with quality system and manage budget for clinical drug supplies.
- 100% Remote Work
- Full-Time
- Employee
- 157,846 - 184,097 USD Annually
- US National
Provide statistical expertise on safety assessment activities, lead statistical activities related to aggregate safety data, collaborate with cross-functional teams, ensure statistical accuracy, adhere to policies and procedures.
- 100% Remote Work
- Full-Time
- Employee
- 169,047 - 206,620 USD Annually
- US National
Develop global launch activities, support pricing governance, and facilitate global access team forum. Conduct situation analysis and payer/pricing research. Collaborate with cross-functional teams and support franchise level initiatives.
- 100% Remote Work
- Full-Time
- Employee
- 125,000 - 300,000 USD Annually
- Canada, Mexico
Grow market adoption of a safety platform, provide sales support, give business guidance to product team, direct resources, present at conferences, and build relationships with stakeholders in the clinical R&D industry.
- 100% Remote Work
- Part-Time
- Employee
- 24.13 - 34.70 USD Hourly
- AZ, FL, GA, IA, KY, MD, MI, MS, NC, OH, PA, SC, TN, VA, WV, WI
Codes, summarizes, and stages extracted information according to complex rules. Conducts quality control activities and creates case abstracts for cancer patients. Responds to requests for information and serves as a liaison within industry and regio..
- 100% Remote Work
- Full-Time
- Employee
- Canada
Perform market landscaping analyses for drug discovery pipelines. Monitor news sources, patents, and company websites for competitive intelligence. Share implications with senior management. Support identifying new drugs for the discovery portfolio.
- 100% Remote Work
- Full-Time
- Employee
- 125,000 - 300,000 USD Annually
- Canada, Mexico
Develop and execute CDMS vision for mid-tier CROs. Drive adoption discussions based on credibility and knowledge across multiple domains. Build deep relationships in the broader community and connect sponsors and partners through Veeva.
- 100% Remote Work
- Full-Time
- Employee
- Sofia, Bulgaria
Create and maintain a database of Key People Profiles. Improve profile structure and data captured. Manage team performance and achieve quality standards. Develop team members and drive process improvements.
- 100% Remote Work
- Full-Time
- Employee
- 125,000 - 300,000 USD Annually
- Canada, Mexico
Develop and execute CDMS vision for mid-tier CROs. Use professional networks and relationships to assist with adoption. Provide thought leadership and sales support to teams in driving adoption of CDMS.
- Hybrid Remote Work
- Full-Time
- Employee
- 130,000 - 190,000 USD Annually
- Palo Alto, CA
Lead site qualification and selection, study initiation visits, and oversee routine monitoring and close-out visit conduct. Develop dashboards and status reports to communicate study status and progress internally and externally.
- Hybrid Remote Work
- Full-Time
- Employee
- 155,000 - 200,000 USD Annually
- New York
Lead statistical strategy and technical activities for drug development, collaborating with cross-functional teams. Develop study designs, evaluate clinical trial designs via simulation, and ensure compliance with data submission guidelines.
- 100% Remote Work
- Full-Time
- Employee
- 215,000 - 296,000 USD Annually
- Hayward, CA, Brisbane, CA, or US National
Lead regulatory strategy for product development, mentor team members, interact with regulatory agencies, manage submissions, and provide training. Regulatory affairs experience required.
- Hybrid Remote Work
- Full-Time
- Employee
- Lawrence Township, NJ
Coordinates cross-functional teams in a country, acts as the main point of contact with the protocol manager and global study team, and develops patient recruitment strategy and risk mitigation. Also coordinates with internal roles for site feasibili..
- 100% Remote Work
- Full-Time
- Employee
- Houston, TX, or US National
Design, plan, and execute clinical studies for medical devices. Manage resources, timelines, and study documentation. Maintain communication with study stakeholders and sites for a collaborative working environment.
- 100% Remote Work
- Full-Time
- Employee
- 85,500 - 182,100 USD Annually
- AR
Provides support and directions to other engineers and scientists in the field of Biological Sciences. Develops and executes project plans, oversees subject matter expertise, and manages external test campaigns.
- 100% Remote Work
- Full-Time
- Employee
- NA, Italy, NA, Cameroon
Providing expert clinical product and technical assistance and training to physicians, laboratory staff, and sales representatives. Educating customers and internal employees on the merits and proper clinical usage of products. Attending cases in lab..
- 100% Remote Work
- Full-Time
- Temporary
- 25.00 - 25.00 USD Hourly
- New York, NY
Create bioinformatics software tools, analyze scientific data, and communicate results with product development teams. Actively pursuing or having a degree in Bioinformatics or related field, with experience in Linux and Python.
- Hybrid Remote Work
- Full-Time
- Employee
- New Brunswick, NJ, Summit West, NJ
Develop global regulatory CMC strategies, assess manufacturing change controls, interpret global regulations, provide technical teams insight into regulatory health authority expectations. BA/BS degree and 3-5+ years pharmaceutical or related experie..
- Hybrid Remote Work
- Full-Time
- Employee
- Field, CO
Develop and maintain relationships with HCPs, answer scientific questions, deliver medical programs, and support clinical trial activities. Provide insights to the medical and commercial organizations. Medical degree and experience in scientific or c..
- Hybrid Remote Work
- Full-Time
- Employee
- Princeton, NJ
Support project teams for pipeline products from development through completion of post-marketing commitments and lifecycle management projects. Provide strategic CMC regulatory expertise and input to development and GO teams. Interpret global regula...
- Hybrid Remote Work
- Full-Time
- Employee
- 159,000 - 220,000 USD Annually
- Princeton, NJ, Cambridge, MA, Brisbane, CA
Drive optimal research portfolio performance, manage research governance planning and execution, collaborate with key stakeholders, support program leadership development, foster cross-functional synergies.
- 100% Remote Work
- Full-Time
- Employee
- US National
Develop and maintain comprehensive CP strategic development plans. Provide CP subject matter expertise to the clinical study team. Supervise and/or conduct pharmacokinetic/pharmacodynamic (PKPD) analyses. Work closely with Regulatory to provide CP su..
- 100% Remote Work
- Full-Time
- Employee
- Canada, or US National
Leads clinical operations, quality aspects, and tool development for studies. Collaborates with clinical team and other departments, ensures timely delivery of clinical deliverables, coordinates start-up activities, and provides resource management input.
- 100% Remote Work
- Full-Time
- Employee
- Lima, Peru, Sao Paulo, Brazil
Manage clinical operations, quality, and finances of assigned studies. Develop monitoring strategy, oversee clinical team, ensure timely delivery of clinical objectives, and implement project-specific processes. Collaborate with project lead and star..
- Hybrid Remote Work
- Full-Time
- Employee
- 82,000 - 102,000 USD Annually
- Brisbane, CA
Contribute to translational projects aligned with CV Translational Research objectives. Conduct laboratory work, literature/data review, and computational analysis. Work independently in cell culture and develop cell-based assays. Present and communi..
- Hybrid Remote Work
- Full-Time
- Employee
- 120,000 - 165,000 USD Annually
- Round Lake, IL
Manage a team of engineers and technicians to support Infusion Systems R&D. Develop robust testing for new product development and on-market product changes. Lead test strategy, planning, and execution for complex electro-mechanical and software devices.
- 100% Remote Work
- Full-Time
- Employee
- Oslo, Norway
Prepare and coordinate regulatory submissions, provide local regulatory strategy advice, maintain trial status information, and ensure local country study files are prepared and maintained. Strong attention to detail and proficiency in English and No..
- 100% Remote Work
- Full-Time
- Employee
- TX
Responsible for providing guidance to assure that all regulatory submissions are planned, communicated, and performed per regulatory and business requirements. Oversee ad/promo reviews to ensure regulatory compliance and support New...
- 100% Remote Work
- Full-Time
- Employee
- 115,000 - 125,000 USD Annually
- Santa Ana, CA
Develop strong business relationships with customers, achieve business objectives, work with a product sales specialist team, and build business strategies to achieve revenue growth targets in the Life Sciences industry.
- Hybrid Remote Work
- Full-Time
- Employee
- Seoul, South Korea
Manages preparation, review, and coordination of country submissions. Provides local regulatory strategy advice and develops local submission strategy. Serves as primary contact for investigators and local regulatory authorities.
- Hybrid Remote Work
- Full-Time
- Employee
- 170,000 - 180,000 USD Annually
- Palo Alto, CA
Develop and create scientifically accurate and impactful materials for the US Field Medical Affairs team. Ensure accuracy, scientific rigor, and alignment with regulatory and compliance standards. Collaborate with cross-functional teams and manage ti..
- 100% Remote Work
- Full-Time
- Employee
- Canada, or US National
Oversee and provide strategic direction for global clinical drug development programs in various therapeutic areas. Ensure operational standards, budgets, and timelines are met. Collaborate with cross-functional teams and stakeholders for successful ..
- 100% Remote Work
- Full-Time
- Employee
- India
Review and customize the Monitoring Report Templates for allocated projects. Evaluate PI oversight, subject safety and study processes in order to assess site's ability to conduct study, as ascertained from information noted in monitoring...
- 100% Remote Work
- Part-Time
- Temporary
- 65.00 USD Hourly
- OR, WA, NV, CA
Design and conduct ADME studies, interpret and report data, collaborate with other teams, and provide input for regulatory documents. PhD in clinical pharmacology/pharmacokinetics-pharmacodynamics with related industry experience r..
- 100% Remote Work
- Full-Time
- Employee
- Argentina, Bolivia, Brazil, Chile, Colombia, Ecuador, Guyana, Paraguay, Peru, Suriname, Uruguay, Venezuela, Mexico
Develop study specific plans, coordinate with internal teams, participate in bidding process, represent department internally and externally, lead process improvement initiatives, consult clients, build strong network, act as backup for functional ma..
- 100% Remote Work
- Full-Time
- Employee
- 28.78 - 59.34 USD Hourly
- Los Angeles, CA
Responsible for regulatory coordination of clinical research studies within assigned units, departments, or divisions. Review clinical research protocols, prepare and manage study/regulatory documents, and ensure compliance with laws and regulations.
- 100% Remote Work
- Full-Time
- Employee
- Toronto, ON, Canada, Halifax, NS, Canada, Edmonton, AB, Canada, Calgary, AB, Canada, Kingston, ON, Canada, London, ON, Canada, Montreal, QC, Canada, Ottawa, ON, Canada, Quebec City, QC, Canada, Regina, SK, Canada, Sherbrooke, QC, Canada, Saint Catherines, ON, Canada
Lead statistical programming activities for clinical research projects, including oversight of dataset creation and report generation. Provide technical expertise, mentor junior programmers, and lead team in working with sponsors on technical process..
- Hybrid Remote Work
- Full-Time
- Employee
- Madison, NJ
Provides disease area expertise/represents BMS USMA CT (internally/externally) in strategic/tactical planning and execution of USMA plans, in strong partnership with the Global Medical Affairs and other cross-functional teams (clinical sub-teams, and..
- Hybrid Remote Work
- Full-Time
- Employee
- Lemont, IL
Develop, manage, and evaluate nonproliferation training activities. Coordinate virtual or on-site trainings, meetings, and projects. Requires knowledge of nonproliferation policies, experience in leading training and research.
- Hybrid Remote Work
- Full-Time
- Freelance
- Seattle, WA
Manage infectious disease clinical trial operations from start to finish, including enrollment, study conduct, close-out, and CSR process. Review study-related documents, guide Clinical Operations team, and oversee project plan, timelines, and budget.
- Hybrid Remote Work
- Full-Time
- Employee
- Cambridge, MA
Utilize in silico prediction tools and conduct in vitro human PBMC-based assays to evaluate immunogenicity potential. Plan and execute experiments, analyze data, and author technical reports. Serve as a representative in cross-functional meetings.
- 100% Remote Work
- Full-Time
- Employee
- 165,000 - 175,000 USD Annually
- US National
Prepare month-end clinical and R&D accruals analysis, review CRO reports, conduct variance analysis, support internal and external reporting requirements, and assist with implementing new accounting software.
- 100% Remote Work
- Full-Time
- Employee
- Canada, Mexico, or US National
Lead cross-functional project team to meet or exceed deliverables. Manage project(s) of increasing complexity. Ensure financial stewardship and compliance with policies, SOPs, ICH-GCP, and regulatory requirements.
- Hybrid Remote Work
- Full-Time
- Temporary
- Seattle, WA
Develop and implement comprehensive project plans, including timelines, milestones, and deliverables. Coordinate and manage project activities, ensuring adherence to timelines, quality standards, and regulatory requirements.
- 100% Remote Work
- Full-Time
- Employee
- Argentina, Bolivia, Brazil, Chile, Colombia, Ecuador, Guyana, Paraguay, Peru, Suriname, Uruguay, Venezuela
Drives and owns the overall delivery of the cross-functional project (time, cost, quality). Ensures financial stewardship at a project level by demonstrating an intimate understanding of the contract, resource alignment to budget...
- 100% Remote Work
- Full-Time
- Employee
- US National
Supervisory responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget, adhering to and promoting principles of delivery and service in dealing with PSI customers...
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