About this role
At Quanticate, we're pioneers in providing top-tier statistical and data management support to clients. We're seeking a dedicated Clinical Data Manager I committed to upholding the highest standards, following procedures, ensuring compliance with regulations, and providing exceptional customer care. You will lead, co-ordinate, and action all tasks relating to Clinical Data Management from start to finish of a study and project manage studies across CDM functions.
Contribute to the efficient running of the CDM department as part of the CDM leadership team. Ensure launch, delivery, leadership and completion of all CDM procedures according to contractual agreement and relevant SOPs, guidelines, and regulations. Pro-actively keep abreast of current clinical data management developments and systems, assist in creation and review of in-house SOPs.
Act as the primary CDM contact both external and internal for Quanticate projects. Manage work assignment and delivery of project tasks to the data processing and programming team. Hold line management responsibilities for assigned direct reports, including professional development, training, and performance appraisals.
Quanticate is the world leading data-focused CRO working on complicated clinical trials requiring high statistical programming, statistics and data management input. Work with top global pharmaceutical companies as an integrated team member or small biotechs taking first steps in clinical development. We advocate career development providing membership to professional societies and encouraging involvement in activities and committees.
Requirements
- Qualified to an appropriate standard, preferably to degree level in a life sciences subject
- Six to Eight years of relevant experience in CRO Clinical Data Management domain, including leading studies
- Extensive knowledge of at least 2 Clinical Data Management systems such as Oracle Clinical, Medidata Rave, Inform
- Thorough knowledge of ICH Guidelines and GCP including regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing
Responsibilities
- Lead, co-ordinate, and action all tasks relating to Clinical Data Management from the start to the finish of a study
- Project manage studies across CDM functions
- Contribute to the efficient running of the CDM department as part of the CDM leadership team
- Ensure launch, delivery, leadership and completion of all CDM procedures according to contractual agreement and relevant SOPs, guidelines, and regulations
- Plan and manage study timelines and resources
- Manage progress against schedules and report to management
- Perform project management across all functions for a study as appropriate
- Manage CRFs and all related tasks
Benefits
- Membership to professional societies
- Involvement in professional societies' activities and committees
- Work as integrated team member on world leading clinical programs with top global pharmaceutical companies
- Support small biotechs taking first steps in clinical development
Similar roles

Real-World Evidence Research Scientist
1w1 week agoNovocure
Haifa, IL · Full-time · ILS 350,000 – ILS 500,000

Statistical Programmer I
1w1 week agoQuanticate
Hyderābād, IN · Full-time · INR 500,000 – INR 800,000

Senior Biostatistician
1w1 week agoClinChoice
US · Full-time · $140,000 – $180,000

Clinical Data Manager / Biomedical Data Specialist (Oncology)
1w1 week agoIndivumed GmbH
Hamburg, DE · Full-time · €55,000 – €75,000