What are the responsibilities and job description for the Associate Clinical Project Manager position at Integrated Resources, Inc ( IRI )?
The Associate Clinical Project Manager (ACPM) supports Clinical Project Managers in the planning, coordination, and execution of Phase I–IV clinical trials from protocol development through study closeout and TMF archiving. This role ensures studies are conducted on time and in compliance with SOPs, ICH-GCP, and regulatory requirements.
Key Responsibilities
- Maintain Trial Master File (TMF) in an inspection-ready state.
- Assist with study documents such as protocols, amendments, informed consent forms, CSRs, and regulatory submissions.
- Coordinate with CROs, vendors, sites, and internal stakeholders.
- Track study timelines, metrics, invoices, and contracts.
- Support clinical data quality, audit readiness, and inspection activities.
- Develop and manage study training materials and compliance records.
- Set up and perform quality checks in CTMS and other clinical systems.
Qualifi cations
- Bachelor’s degree in Life Sciences or related field.
- 1–2 years of CRA or related clinical research experience.
- Knowledge of Phase I–IV clinical trials, ICH-GCP, and regulatory requirements.
- Proficiency in CTMS, TMF/eTMF, Microsoft Office, SharePoint, and Teams.
- Strong organizational, communication, and stakeholder management skills.
Note: Candidates must use their own personal laptop, as the client will not provide equipment.
Salary : $80 - $85