Senior Lead Clinical Data Manager
IDDI (International Drug Development Institute), founded in 1991, is a highly recognized Biostatistical and eClinical data services provider in the field of clinical research, providing agile clinical trials services for pharmaceutical, biotechnology, and medical device/diagnostic companies. Together, we want to achieve one objective: support our clients to accelerate the delivery of their drugs and improve people’s health.
To support our growth and commitment to quality and innovation, we are actively looking for a passionate, proactive, and scientifically-driven individual to reinforce our team in Belgium (Ottignies) for an important role as a:
Senior Lead Clinical Data Manager
As Senior Lead Clinical Data Manager (CDM), you will be responsible for the end-to-end data management process for complex medical research projects in a diverse range of therapeutic areas.
You will play a key role in managing, coordinating, and performing all data management activities for responsible projects. You will ensure on-time delivery of high quality and accurate data to facilitate statistical analysis. You will also ensure data are kept secure throughout the full process of data collection.
You will work very closely with the Biostatistical Services team, and will be the CDM primary contact for all other IDDI stakeholders, as well as the study Sponsor in this critical client facing role.
By participating in the regular review of CDM processes, you will play an active role in the continuous improvement of our operational excellence, both in the CDM team and at IDDI in general.
Based on your expertise, you will coach and train your peers to improve the quality and efficiency of our data management services.
Your key responsibilities:
- Manage and coordinate all activities related to Data Management during the clinical trial to ensure the project’s schedule is respected. This involves regular contact with all CDM team members (i.e., EDC specialists, Programming specialists, Data cleaning and coding specialists)
- Produce and maintain key study related CDM documentation
- Ensure the CRF (Case Report Form) meets the data collection requirements of the study through a review of the protocol and other supporting documentation
- Define and review edit-checks included in the Data Validation Plan in agreement with the study Sponsor
- Ensure external data (e.g., labs, serious adverse events) are transferred and reconciled with the clinical database
- Perform database unblinding and lock activities in close collaboration with the Sponsor, Project Manager, Biostatistician, and other parties
- Develop Data Management standards (templates and processes)
- Communicate proactively with the sponsor and other project collaborators about data management activities status and potential issues.
The successful candidate must have a Master’s degree in the life sciences or a health-related field and at least 5 years of experience in a similar position.
In addition, the position requires:
- Knowledge of EDC systems such as RAVE (Medidata) or MARVIN (EvidentIQ)
- Demonstrated working experience in SAS programming and CDISC standards
- Excellent knowledge of English, both oral and written
- Good planning and analytical skills
- Excellent communication skills
- Ability to work in a fast-paced and regulated research environment
You will join an international and multi-cultural company that includes over 25 different nationalities (English is the working language) and where employees are the strongest asset.
At IDDI, we offer job stability and growth opportunities through on‑the-job training and mentoring programs. Working at IDDI will bring you an expertise that is widely recognized in our industry.
Our customers value our flexibility, responsiveness, and proactive approach.
A unique opportunity to work in a friendly, team-oriented, and stimulating environment. We regularly enjoy company-wide events, such as BBQs, family-day outings, sports, and charity fundraisers – giving the chance to share time together.
We offer a competitive salary and benefits package, including meal vouchers, full reimbursement for public transport, hospital insurance, etc. as well as flexibility for a better work-life balance (flexible working hours with home-working opportunities, part-time schedules).
Interested in this challenging position?
Please send your CV and cover letter highlighting your motivation and relevant professional experience for the position by e-mail at firstname.lastname@example.org (to the attention of Ms. Vanessa Closset)