Clinical Research Manager (Sponsor-dedicated)
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 18h ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 10d ago
The date the source published, not the day we noticed it (2026-10-23). Last seen at its source 2h ago.
We have tracked this listing since 23 Oct 2026 (10 days). The employer's own board has carried it every time we have read it, most recently 2 hours ago.
Is it remote?
Remote Netherlands
That is the location the employer filed this posting under. Quoted as written — we do not re-word the source's own location.
Who may apply?
The Netherlands
The description states no restriction of its own. This is the source's own tag.
Pay not stated
Similar roles pay $30–58/hr
Middle 50% of 25 listings that do state pay — Healthcare · all levels · EMEA · USD/hour. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
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Workday employer's own board first seen 10d ago · last seen 2h ago
The listing
Clinical Research Manager (CRM)
Location: Hybrid, Client Office (as assigned)
About the Role
As a Clinical Research Manager, you’ll lead and oversee local clinical trial operations, ensuring regulatory and financial compliance while driving performance across protocols. You’ll be the key point of contact for investigators and external partners, representing the client and building strong relationships that support trial success.
This role combines strategic oversight with hands-on execution, requiring strong leadership, scientific knowledge, and the ability to manage multiple priorities in a dynamic environment.
Key Responsibilities
- Trial Oversight: Ensure protocol compliance and performance across assigned studies.
- Stakeholder Management: Serve as the primary contact for investigators, vendors, and internal teams.
- Quality & Compliance: Monitor site activities, review reports, and address training needs.
- Operational Leadership: Oversight of budgets, contracts, and resource forecasting.
- Cross-Functional Collaboration: Align with regulatory, PV, medical affairs, and global teams.
What You Bring
- Master’s degree in life sciences or related field (or equivalent experience).
- 6–8 years of clinical research experience in pharma, CRO, or healthcare.
- Previous monitoring experience is needed.
- Strong knowledge of ICH-GCP, local regulations, and clinical trial processes.
- Excellent communication, organizational, and leadership skills.
- Ability to manage multiple protocols and lead cross-functional teams.
- Fluent in English and Dutch (written and spoken).
Preferred Skills
- Experience with site selection, start-up, and vendor management.
- Proven ability to mentor junior staff and foster team performance.
- Comfortable working independently and in virtual environments.
Learn more about our EEO & Accommodations request here.