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Clinical Trial Manager

5+ years
Not Disclosed
10 Feb. 25, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Trial Manager (6 Months Contract)

Location: South San Francisco, CA (3 days in-office per week)
Employer: Meet
Employment Type: Contract
Seniority Level: Mid-Senior Level
Job Function: Science and Research
Industries: Staffing and Recruiting, Biotechnology Research, Pharmaceutical Manufacturing


Position Overview:

Meet is seeking a Clinical Trial Manager to support the operational execution of Phase I and early-phase clinical trials. This role involves overseeing site activation, patient recruitment, study management, and vendor oversight, ensuring that clinical studies are executed successfully in collaboration with internal teams, CROs, and external partners. The trials you will support are crucial to the development of innovative treatments aimed at improving patient outcomes.


Key Responsibilities:

  • Study Execution: Support Phase I and early-phase clinical trials by managing study setup, budget tracking, milestones, and timelines.

  • Site Management: Assist with site feasibility, recruitment, and preparation of clinical study documents (protocols, ICFs, etc.) in compliance with ICH/GCP guidelines.

  • Vendor Oversight: Manage vendor relationships for systems like EDC, IRT, and specialty services.

  • Monitoring: Provide monitoring support and track study progress, keeping senior management informed.

  • Stakeholder Communication: Build and maintain strong relationships with investigators and study personnel.


Professional Qualifications:

  • Regulatory Knowledge: Strong understanding of US and global regulations, including SOPs, ICH-GCP, FDA-CFR.

  • Skills: Excellent time management, organizational, and multitasking abilities.

  • Technology Proficiency: Experience with Microsoft Office, Smartsheet, eTMF, and clinical technologies.

  • Documentation Management: Ability to manage clinical study documentation and oversee risk management strategies.


Education & Experience:

  • Education: B.S. or advanced degree in biological sciences or a related discipline.

  • Experience: Minimum of 5 years of clinical trial management experience, preferably within pharma, biotech, or CRO environments.


Why Apply?

This is an excellent opportunity for a Clinical Trial Manager to gain exposure to early-phase clinical trials while contributing to the development of life-saving treatments. If you have a strong background in clinical trial management and are looking to make an impact, this role could be a perfect fit for you.