Global Clinical Trials Disclosure Lead

Wodker Associates; Barcelona; On-site; EUR 60,000 - 90,000; Full time

Job summary

Wodker Associates in Barcelona, Spain, seeks a CTP Manager to oversee disclosure of clinical trial information across registries and public websites, ensuring compliance with internal rules and external guidelines. You will develop and update the disclosure strategy, perform QA checks, and coordinate data collection and posting on company sites, with emphasis on accuracy and regulatory adherence.

This role requires an advanced degree in Medicine or Life Sciences and 2–3 years in trial

Qualifications

• Advanced degree in Medicine, Life Sciences, or Natural Sciences or equivalent long-term professional experience.
• Min. 2 - 3 years experience in clinical trial disclosure with significant experience related to the conduct and analysis of clinical trials.
• Advanced understanding of global legislations, regulations and guidelines.
• Advanced understanding of ICH/GCP regulations.
• Strong English language skills, fluent speaking mandatory.
• Advanced knowledge of the co product and development portfolio.
• Solid understanding of cross-divisional business requirements of R&D functions and other internal customers.

Responsibilities

• Disclose clinical trial information on registries and websites with accuracy and timeliness.
• Ensure QA of disclosed information per internal processes.
• Monitor and update disclosure strategies to meet evolving laws and guidelines.
• Check for promotional language and internal compliance in disclosures.
• Coordinate data collection and posting across platforms.

Skills

Clinical trial disclosure

Regulatory compliance

Quality Assurance

Project management

English proficiency

Education

Advanced degree in Medicine

Life Sciences degree

Tools

Clinical Trial Management Systems

Workflow Management Systems

Job description

Wodker Associates in Barcelona, Spain, seeks a CTP Manager to oversee disclosure of clinical trial information across registries and public websites, ensuring compliance with internal rules and external guidelines. You will develop and update the disclosure strategy, perform QA checks, and coordinate data collection and posting on company sites, with emphasis on accuracy and regulatory adherence.

This role requires an advanced degree in Medicine or Life Sciences and 2–3 years in trial