2 дня назад
Clinical Trials Project Manager
80 000 - 100 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Trials Project Manager (Clinical Research/Laboratory Operations): Managing clinical trial protocols from setup through maintenance and closeout while coordinating clients, investigators, and internal laboratory functions with an accent on regulatory documentation, study metrics, and client delivery. Focus on developing laboratory specifications and work instructions, conducting investigator training, solving study issues, and maintaining compliance with FDA, GCP, ICH, and other applicable regulations.
Location: Remote, United States; occasional overnight travel to client events, investigator meetings, and international ACM locations is required.
Salary: $80,000–$100,000 per year.
Company
provides central laboratory services supporting clinical trials and their associated study management activities.
What you will do
- Serve as the primary client contact for the laboratory aspects of assigned clinical trials.
- Manage approximately 10–25 protocols after training, including trials with more than $3 million in contract value.
- Coordinate study setup, maintenance, closeout, troubleshooting, and problem-solving across internal functions.
- Develop global laboratory specification documents, investigator manuals, and protocol-specific work instructions.
- Review project metrics and budgets, support quality audits and inspections, and maintain regulatory documentation.
- Conduct investigator training sessions, provide on-call coverage, and travel to client and investigator events as required.
Requirements
- At least 1 year of project management experience.
- General working knowledge of FDA, NYSDOH, GCP, ICH, and other regulations relevant to central laboratory functions.
- Ability to travel overnight, including occasional weekend travel, and maintain valid passport qualifications.
- Ability to manage confidential patient and client information and perform prolonged computer-based work.
- Must be based in the United States for this remote role.
Nice to have
- Bachelor’s degree.
- Experience in clinical trials, laboratory, or healthcare settings.
- Strong problem-solving and communication skills.
Culture & Benefits
- Full-time schedule of 40 hours per week, Monday through Friday.
- Remote work arrangement with occasional travel to client events and ACM locations.
- Potential flexible hours and on-call coverage duties.
- Work is performed in a sedentary, office-based environment with accommodations considered for reported physical requirements.
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