Data Manager

CK Group
16 days ago

Role details

Contract type
Temporary contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English
Experience level
Intermediate

Job location

Remote

Tech stack

Clinical Data Management
Databases
Coherent Remote File System (CRFS)
Data Streaming
Data Management

Job description

CK QLS are seeking a dedicated and detail-oriented Data Manager to join our team in Allschwil, Switzerland. This is a full-time position with a 24-month duration, starting in Q1 2026. As a Data Manager, you will play a pivotal role in ensuring the integrity and compliance of data management activities within clinical research., * Ensuring all Data Management activities adhere to internal standards and regulatory requirements.

  • Supporting the development and testing of (e)CRFs and data review tools.
  • Contributing to the creation and maintenance of Data Management documentation.
  • Performing data review, managing discrepancies and queries, and tracking protocol deviations.
  • Assisting in database lock activities and providing metrics to the Project Data Manager.
  • Archiving study documentation in compliance with established guidelines., * Collaborate with cross-functional teams to ensure data accuracy and compliance.
  • Develop and test electronic Case Report Forms (eCRFs) and data review tools.
  • Review and manage clinical trial data, addressing discrepancies and queries.
  • Track protocol deviations and ensure proper documentation.
  • Provide metrics and updates to the Project Data Manager.
  • Archive study-related documentation in line with regulatory and internal standards.

Requirements

Do you have experience in Organizational skills?, Do you have a Bachelor's degree?, * A Bachelor's degree or higher in a pharmaceutical or biomedical discipline (e.g., Biological Sciences, Pharmacology).

  • A minimum of 2 years of experience in Clinical Research or Clinical Data Management within the Pharmaceutical or Biotech industry.
  • A solid understanding of clinical trial databases, data flow, and (e)CRF design.
  • Familiarity with ICH-GCP and international clinical research regulations.
  • Strong organizational skills and a collaborative mindset.
  • Fluency in written and spoken English.

Benefits & conditions

We offer a supportive and inclusive work environment with the following benefits:

  • A friendly and collaborative working atmosphere.
  • The flexibility to work from home up to 2 days per week.
  • Opportunities to work on exciting projects in an international setting.

We are committed to fostering diversity and inclusion in the workplace and encourage candidates from all backgrounds to apply. If you are passionate about making a difference in clinical research and meet most of the qualifications, we encourage you to apply. Join us in shaping the future of healthcare and contributing to meaningful projects that impact lives globally.

It is essential that applicants hold entitlement to work in Switzerland. Please quote job reference 161119 in all correspondence.

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