Chief Data Officer

Optimapharm is a globally operating, leading, mid-sized, full-service CRO aiming to deliver new therapies to improve and save patients’ lives.
Optimapharm’s key priorities are the well-being of our people, consistent quality delivery to our clients and healthy, sustainable growth.
Established nearly 20 years ago, we leverage our experience, stable project teams and collaborative, and flexible approach to secure a high level of repeat business, gain the trust of new customers and secure continued growth of the company.
As a Senior Data Manager at Optimapharm, you’ll be at the forefront of driving data excellence in clinical research. You won’t just manage data; you’ll lead projects, guide teams, and shape the standards that ensure our studies deliver reliable, meaningful results. Partnering closely with cross-functional experts, you’ll play a critical role in transforming complex clinical data into insights that advance science, support our sponsors, and ultimately improve patients’ lives worldwide.
&##International projects and professional growth
Performance bonus
Training and development opportunities
Bachelor’s or higher degree in a biomedical or technical field (e.g., 3-5 years of proven experience in Clinical Data Management within CRO, pharma, or biotech settings.

• Strong understanding of quality systems and regulatory compliance
• Proficient in EDC systems and database standards (e.g., SQL); knowledge of programming languages such as Python, R, SAS, or VBA is an advantage
• Effective communicator and team player with the ability to manage multiple projects and deadlines

&##Lead and oversee end-to-end data management activities across assigned clinical studies
Ensure data accuracy, integrity, and compliance with study protocols and regulatory standards
Develop, review, and maintain key data management documents (DMPs, CRFs, edit checks, transfer specs)
Design, test, and validate EDC systems and related databases, including user acceptance testing
Manage and coordinate data cleaning, reconciliation, and database lock activities
Perform and oversee medical coding of adverse events and medications using standard dictionaries
Act as the main point of contact for sponsors, vendors, and internal project teams
Provide leadership, guidance, and mentorship to data management team members
Participate in audits, inspections, and quality improvement initiatives
Monitor project timelines, deliverables, and KPIs, ensuring on-time and within-budget delivery
Stay current with industry trends, technologies, and regulatory updates in clinical data management
If you would be interested in joining the Optimapharm team, please send your CV in English and note that only shortlisted candidates that meet the requirements will be contacted for the further selection process.