Clinical Trials Associate Project Manager
ACM Global Laboratories · United States · US
Clinical Research
Remote
physician
Demand78
Career growth72
Healthcare fit82
Remote potential25
Salary band
USD 65k – 85k
5-year outlook
Realistic growth into clinical trial project management, central lab client management, or CRA/clinical operations roles; compensation should rise with study complexity, therapeutic area exposure, and PM ownership, though exact figures depend on location and employer.
Clinical license
Not required
Applicant reach
broad
Seniority
entry
Employment type
full-time
Date found
2026-10-19
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- License jurisdiction
- US
- Profession fit
- physician
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth applying for clinicians or healthcare graduates who want to move into clinical research operations and are comfortable with client-facing project coordination, regulatory documentation, and on-call duties. It is a practical entry point into clinical trials project management, especially for those with at least one year of healthcare, lab, or trials exposure.
Who should apply
Nurses, pharmacists, allied health professionals, IMGs, and healthcare graduates with at least one year in a clinical, laboratory, or clinical trials setting who want non-bedside clinical research project management experience.
CV angle
Frame real clinical or laboratory experience around clinical trial support, protocol familiarity, GCP/ICH/FDA awareness, regulatory documentation, quality audit readiness, stakeholder communication, timeline tracking, and budget/metrics review. Emphasize any exposure to study start-up, site or lab coordination, patient confidentiality, and cross-functional troubleshooting without overstating project management ownership.
Skills to highlight
- Clinical trial coordination
- Project management support
- GCP/ICH/FDA regulatory awareness
- Central laboratory workflows
- Client and stakeholder communication
- Regulatory documentation and archiving
- Quality audit support
- Budget and metric tracking
Role summary
An entry-level clinical trials project management role at a central laboratory, coordinating low-complexity studies from setup through close-out, acting as client point of contact, developing protocol-specific lab documents, supporting audits, tracking budgets and metrics, and ensuring regulatory compliance.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.