Randstad Professional
Clinical Trial Disclosure Lead (m/w/d)
Monheim am Rhein, Nordrhein-Westfalen, Germany
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hirly's read of this role
- Role family
- Healthcare
- Seniority
- Lead / management
- Country
- DE
- Work mode
- On-site / unstated
- First seen by hirly
- 26 Sept 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
- Randstad is one of the world's leading talent companies with the
- ambition to be the world's most equitable and specialized talent
- company. Through our "partner for talent" corporate strategy, we find,
- develop and connect specialized talents with companies - worldwide,
- locally and always at a high speed. We build high-quality, diverse,
- and agile teams, while individuals can enjoy a rewarding career path
- with equitable opportunities.
- Randstad Professional is one of Randstad's four specializations
- and focuses on the placement of specialists and managers in the
- future-oriented sectors of IT, Engineering, Life Science and Office.
- Are you passionate about transparency in clinical research and eager
- to ensure that global study data meets the highest regulatory
- standards?
- We are currently looking for a Clinical Trial Disclosure Lead (m/f/d)
- for our pharmaceutical client in Monheim am Rhein (fully remote
- possible). In this role, you will independently manage the entire
- process of clinical trial registration and results disclosure at the
- study level.
- This position is available via temporary employment
- (Arbeitnehmerüberlassung) for 18 months, with the option of contract
- extension.
- Strategy & Planning: Define disclosure strategies early at
- study concept, protocol, and amendment stages.
- Registrations & Submissions: Prepare, review, and submit clinical
- trial registrations across global registries such as CTIS and
- ClinicalTrials.gov.
- Lifecycle Management: Maintain accurate, up-to-date, and compliant
- registry records throughout the entire study lifecycle.
- Results Disclosures: Coordinate the creation and submission of
- clinical trial results disclosures.
- Compliance & Audits: Ensure full inspection readiness through
- precise documentation and auditable evidence.
- Operations & Oversight: Support data quality, system maintenance,
- and vendor oversight activities.
- Remote: 3 days/week or 100% remote possible
- Education & Experience: Degree in Life Sciences (or a related
- discipline) with a background in clinical research, trial management,
- Regulatory Affairs, or project management.
- Technical Expertise: Knowledge of clinical trial transparency and
- disclosure requirements, familiarity with registries such as CTIS or
- ClinicalTrials.gov, and strong affinity for IT systems. (Experience at
- a CRO or Sponsor is a plus).
- Languages: Fluent English (must-have); German skills are a
- nice-to-have.
- Soft Skills: High attention to detail, strong organizational
- skills, proactive communication, and an open, collaborative mindset.
- Attractive salary and long-term job security through affiliation
- with the Group
- Up to 30 days vacation per year
- Good chances of being taken on by our business partners
- Targeted training opportunities and free language courses
Listed on hirly, a job board. hirly is not the employer: Randstad Professional is hiring for this role.
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