Project Management Associate (PMA)
TFS HealthScience · Czechia, Finland, France, Hungary, Italy, Netherlands, Poland, Portugal, Spain, United Kingdom · GB
Clinical Research
Remote
Not yet analysed
Demand75
Career growth72
Healthcare fit70
Remote potential65
5-year outlook
A realistic path toward Clinical Trial/Project Management roles in CROs, with salary growth tied to study complexity, therapeutic area, and regional market rates; exact figures vary and are not stated in the posting.
Clinical license
Not required
Applicant reach
moderate
Seniority
entry
Employment type
full-time
Date found
2026-10-26
Intelligence details
Flexible work details
- Engagement type
- Contract
- Hours
- Variable hours
- Eligible countries
- United Kingdom
- Rate period
- Annual
Why this was classified this way
- Contract
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 considering for clinicians who want a structured entry into CRO project management and already have some clinical research, CTA, or study coordination exposure. Clinicians without CRO/CTA experience should apply only if they can clearly demonstrate transferable trial documentation, coordination, and Excel skills.
Who should apply
Clinicians and healthcare graduates with clinical trial exposure, research coordination experience, or CTA internships who want to move into CRO project management; nurses, pharmacists, doctors, IMGs, and allied health professionals with strong organizational and Excel skills.
CV angle
Reframe real clinical and research experience around study coordination, documentation accuracy, regulatory compliance, stakeholder communication, tracker management, and audit/inspection readiness. Highlight any exposure to CTMS, clinical trial sites, investigator communications, vendor or invoice tracking, and advanced Excel use; do not claim CRO experience you do not have.
Skills to highlight
- Clinical trial coordination and study documentation
- CTMS and study file maintenance
- Advanced Excel including pivot tables and macros
- Project coordination and meeting management
- Vendor management and invoice/payment tracking
- Regulatory submission and audit support
- Stakeholder communication in client-facing settings
- AI tools for process efficiency
Role summary
An entry-level CRO project management support role focused on clinical study administration, documentation, trackers, meeting coordination, vendor and payment support, regulatory submissions, and communication with study teams and sponsors.
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