Remote Senior Clinical Trial Lead

Precision Medicine Group

United States

Remote

USD 111,000 - 201,000

Full time

14 days+

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Benefits offered by this job

Discretionary annual bonus
Health insurance
Retirement savings
Life insurance
Disability benefits
Parental leave
Paid time off

Job summary

Precision Medicine Group is seeking a Clinical Trial Manager/Senior Clinical Trial Manager for a remote role in the United States. You will lead the operational aspects of clinical studies, drive feasibility, budgeting, and regulatory submissions, and mentor CRAs and CTAs to ensure timely, compliant trial delivery.

Requirements include a Bachelor’s degree in science/health, 7+ years of clinical research experience, and strong knowledge of ICH-GCP and SOPs.

Qualifications

  • Bachelor’s degree or equivalent in science/health; advanced degree preferred.
  • Minimum 7 years clinical research experience or proven monitoring competencies.

Responsibilities

  • Serve as clinical trial lead for planning, conduct and oversight per scope of work.
  • Collaborate with PM on monthly invoicing and budget variance management.
  • Develop study documents (plans, ICF templates, CRF guidelines, manuals).
  • Identify training needs for CRAs and vendors; present at Investigator Meetings.
  • Drive site feasibility and recruit/retention strategies across countries.
  • Ensure regulatory submissions and IP release packages are reviewed and approved.

Skills

Communication skills
Team leadership
Time management
Negotiation
ICH-GCP knowledge
Cross-functional
Regulatory compliance

Education

Bachelor's degree in science/health
Advanced degree

Tools

Microsoft Office
CTMS
eTMF systems

Job description

Precision Medicine Group is seeking a Clinical Trial Manager/Senior Clinical Trial Manager for a remote role in the United States. You will lead the operational aspects of clinical studies, drive feasibility, budgeting, and regulatory submissions, and mentor CRAs and CTAs to ensure timely, compliant trial delivery.

Requirements include a Bachelor’s degree in science/health, 7+ years of clinical research experience, and strong knowledge of ICH-GCP and SOPs.

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