Data Manager
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Job Location:
Arlesheim - Switzerland
Monthly Salary:
Not Disclosed
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
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.
Responsibilities:
As a Data Manager your key responsibilities will include:
To excel in this role you should possess the following qualifications and skills:
On a typical day you will:
We offer a supportive and inclusive work environment with the following benefits:
It is essential that applicants hold entitlement to work in Switzerland. Please quote job reference 161119 in all correspondence.
INDSW
Responsibilities:
As a Data Manager your key responsibilities will include:
- 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.
To excel in this role you should possess the following qualifications and skills:
- A Bachelors 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.
On a typical day you will:
- 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.
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.
It is essential that applicants hold entitlement to work in Switzerland. Please quote job reference 161119 in all correspondence.
INDSW
Company Industry
Pharmaceuticals
About Company
Idibu
100 employees
Every business is now operating in an environment that’s susceptible to change. idibu has evolved against this changing backdrop. Whether driven by legislation, technology, customer demand or the economy, businesses now need to be agile and fleet of foot to ensure they can attr ... View more
