Project Coordinator I, Phase I
New
F
FortreaClinical Research
All candidates must reside in the United States.Full-TimeEntry
Salary28 - 30 USD per hour
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Job Details
- Experience
- 2–3 years of clinical research experience
- Required Skills
- Project ManagementGCP
Requirements
- Degree in life sciences or related field (or equivalent experience).
- 2–3 years of clinical research experience, ideally in early phase studies.
- Experience supporting project management or study coordination.
- Knowledge of GCP/ICH guidelines and clinical trial processes.
- Strong organizational, communication, and problem-solving skills.
- Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
- Regular and consistent attendance.
Responsibilities
- Coordinate and support delivery of Phase I clinical trials, including external site studies.
- Develop and maintain key study documents (project plans, communication plans, risk registers).
- Track timelines, milestones, and study progress to ensure successful execution.
- Lead and support study meetings, including agendas, minutes, and follow-up actions.
- Manage systems such as CTMS and eTMF, ensuring accuracy and compliance.
- Act as a key point of contact for internal teams and external sites.
- Support feasibility, start-up activities, and vendor coordination.
- Contribute to continuous improvement initiatives and help mentor junior team members.
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