Lead Clinical Trial Manager — Drive Timelines & Quality

Precision Medicine Group

San Francisco (CA)

Hybrid

USD 140,000 - 190,000

Full time

14 days+

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Precision Medicine Group in San Francisco seeks a Clinical Trial Manager to lead the clinical team on a study, ensuring timeline adherence, proper scope, and quality delivery. You will thrive in a fast-paced, collaborative environment and partner closely with sponsors and internal teams to drive successful trials.

Responsibilities include feasibility, site selection, startup, enrollment, monitoring plans, data cleaning, and close-out.

Qualifications

Bachelor’s degree or equivalent combination of education/experience in science or health-related field.
Clinical Trial Lead/Manager: Minimum of 5–7 years of clinical research experience with significant monitoring experience.

Responsibilities

Management and operational delivery of the clinical elements within a trial, including site feasibility and selection, start-up, clinical plans and document development, subject enrollment, site engagement and support, monitoring planning and execution, resourcing, regulatory documentation, data cleaning activities, and close-out.
Successful execution of assigned trials and ensuring completion of trial deliverables.
Ensuring appropriate communication and ongoing oversight of assigned trial(s) by working in close collaboration with the sponsor and other functional team members.
Participation in sponsor meetings and presentations.
Mentoring and training team members.
Leading CRAs as they establish relationships with their sites for high quality oversight.
Contribute to company and department initiatives to grow processes and the PFM overall.