Clinical Research Specialist - Fully Remote

Mercor; Canada; Remote; CAD 100,000 - 140,000; Full time

Job summary

A leading technology and research firm is seeking a Clinical Trial Design Specialist to lead designing and developing clinical trials for cardiovascular therapeutics. The role emphasizes innovative methodologies and compliance with regulatory guidelines. Candidates should have an advanced degree and over 5 years of experience in clinical trial design. Remote work is available, offering global exposure.

Qualifications

• 5+ years of experience in clinical trial design and development, preferably in cardiovascular disease.
• Proven experience in protocol writing and regulatory interactions.
• Strong understanding of drug development across small molecules and biologics.

Responsibilities

• Lead the design, protocol development, and statistical framework for clinical trials.
• Collaborate with clinical and regulatory teams to optimize trial endpoints.
• Ensure compliance with FDA, EMA, and ICH guidelines.

Skills

Clinical trial design

Protocol writing

Collaboration

Regulatory compliance

Biostatistics

Communication

Education

Advanced degree (MD, PhD, PharmD, or MSc) in Clinical Research, Medicine, or Life Sciences

Job description

Overview

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.

Role Overview

• 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.

Responsibilities

• 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.

Qualifications

• 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.

Engagement Details

• Flexible engagement opportunities: Consulting or full-time
• Remote work available
• Global exposure

Application Process

• Upload resume
• AI interview based on your resume
• Submit form

Resources & Support

• 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: [e-mail]

PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.