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Clinical Research Scientist
Job summary
A leading clinical research organization is seeking a Clinical Trial Design Specialist to design and develop innovative cardiovascular trials. This role offers flexible engagement opportunities, including consulting and full-time, and allows remote work. The ideal candidate has extensive experience in clinical trial design, protocol writing, and regulatory interactions, ideally in the field of cardiovascular therapeutics.
Qualifications
- 5+ years of experience in clinical trial design and development, preferably with cardiovascular disease.
- Strong understanding of drug development across small molecules, biologics, and novel therapeutics.
- Excellent writing and communication skills for multidisciplinary teams.
Responsibilities
- Lead the design and protocol development for cardiovascular trials.
- Collaborate with experts to optimize trial endpoints and patient selection.
- Ensure compliance with FDA, EMA, and ICH guidelines.
Skills
Education
Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey.
- Position: Clinical Trial Design Specialist – Contract, Remote
- Commitment: Flexible engagement opportunities (consulting or full-time)
- Focus on designing and developing clinical trials for cardiovascular therapeutics. Emphasizes innovative methodologies and compliance with regulatory guidelines.
- Lead the design, protocol development, and statistical framework for Phase I–III cardiovascular and inflammatory disease trials.
- Collaborate with clinicians, regulatory experts, and biostatisticians to optimize trial endpoints, patient selection, and study power.
- Ensure compliance with FDA, EMA, and ICH guidelines for trial design and execution.
- Review and incorporate real-world evidence, biomarkers, and emerging trial methodologies into study planning.
- Support cross-functional teams in regulatory submissions, trial monitoring, and results interpretation.
- Provide expertise in risk mitigation, adaptive trial design, and innovative methodologies.
- Must-have qualifications: Advanced degree (MD, PhD, PharmD, or MSc) in Clinical Research, Medicine, or Life Sciences.
- 5+ years of experience in clinical trial design and development, with cardiovascular disease experience strongly preferred.
- Proven experience in protocol writing, endpoint selection, and regulatory interactions.
- Familiarity with biostatistics, trial modeling, and adaptive design methodologies.
- Strong understanding of drug development across small molecules, biologics, and novel therapeutics.
- Excellent collaboration, writing, and communication skills for multidisciplinary teams.
- Flexible engagement opportunities: Consulting or full-time
- Remote work available
- Global exposure
- Upload resume
- AI interview based on your resume
- Submit form
- For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome/welcome
- For any help or support, reach out to: support@mercor.com
PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.
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