Project Manager
Alira Health · Italy
Clinical Research
Remote
Pharmacist
Demand78
Career growth72
Healthcare fit72
Remote potential65
Salary band
EUR 50k – 70k
5-year outlook
Clinical research project management offers stable progression into senior PM, clinical program management, or sponsor-side roles; compensation typically grows with CRO/sponsor experience and therapeutic area expertise, though exact figures vary by region.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-10-02
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Contract
- Hours
- Variable hours
- Profession fit
- Pharmacist
- 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 applying for clinicians with CRO, pharma, or clinical trial coordination experience who want a non-clinical project management path. Clinicians without industry trial experience may find the 3-year CRO/pharma requirement a significant barrier.
Who should apply
Research nurses, pharmacists, physicians, and IMGs with clinical trial coordination, GCP, or CRO/pharma experience; life sciences graduates with clinical research exposure.
CV angle
Reframe clinical experience around trial coordination, patient recruitment/retention, protocol adherence, GCP compliance, data collection, multidisciplinary collaboration, and any budget/timeline or team leadership responsibilities. Quantify study volumes, site coordination, and stakeholder communication.
Skills to highlight
- Clinical trial coordination
- ICH GCP compliance
- FDA regulatory knowledge
- Project management
- Sponsor and vendor communication
- TMF management
- Budget and timeline management
- Cross-functional team leadership
Role summary
Project Manager at a clinical research organization, responsible for leading clinical studies from start-up through close-out, managing sponsors, vendors, budgets, timelines, and clinical team members while ensuring ICH GCP and FDA compliance.
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