Clinical Data Manager II Senior Clinical Data Manager

About the Role

Precision for Medicine is seeking a highly skilled and motivated Clinical Data Manager II or Senior Clinical Data Manager to join our growing global team. This role is designed for a clinical research professional who thrives in a fast-paced environment and is passionate about ensuring data integrity within the pharmaceutical and biotechnology sectors. As a vital member of our organization, you will be responsible for the strategic and operational management of data processes, ensuring that clinical trial data is collected, managed, and reported with the highest levels of accuracy and regulatory compliance. We are looking for candidates based in the United Kingdom, Poland, Hungary, Romania, Serbia, or Slovakia who are ready to take on a lead role and drive successful outcomes for our global partners.

In this senior-level role, you will act as the Primary Data Management (Lead DM) contact for assigned clinical projects and programs. You will be responsible for maintaining continuity, responsiveness, and timeliness across all data-related tasks. Your core duties will include:

• Managing the full lifecycle of clinical trial data management from study start-up through post-database lock, ensuring adherence to project timelines and quality standards.
• Overseeing and performing database development, including the design, testing, and validation of Electronic Data Capture (EDC) systems.
• Developing study-specific plans, including Data Management Plans (DMP), Data Validation Specifications, and Case Report Form (CRF) completion guidelines.
• Ensuring all activities are conducted in strict accordance with Standard Operating Procedures (SOPs), Work Instructions (WIs), and international regulatory directives such as GCP and ICH.
• Supervising the project data entry process, providing training to investigative sites and internal staff, and managing resourcing needs for assigned projects.
• Leading data cleaning activities, including query management, medical coding oversight, and external data reconciliation.
• Performing comprehensive quality control reviews of data entry and overall database health to identify trends or risks early in the study lifecycle.
• Providing mentorship and oversight to junior team members or supporting other Lead DMs as a backup or collaborative team member on large-scale programs.
• Collaborating closely with clinical operations, biostatistics, and project management teams to ensure seamless data flow and reporting.

To succeed in this role, you must demonstrate a deep understanding of clinical data management principles and the ability to lead complex projects independently. We are looking for candidates with the following qualifications:

• A Bachelor's degree in a life sciences, computer science, or a related field; or equivalent professional experience.
• Significant experience in clinical data management (CDM) within a CRO or pharmaceutical environment, with a track record of success at a Level II or Senior level.
• Extensive knowledge of EDC platforms such as Medidata Rave, Veeva, or Oracle Clinical, including experience with database development workflows.
• Strong familiarity with industry standards, including CDISC (CDASH, SDTM) and regulatory requirements for clinical trial data.
• Excellent project management skills with the ability to manage multiple priorities and meet strict deadlines in a high-pressure, remote environment.
• Superior communication skills in English, both written and verbal, to effectively collaborate with global cross-functional teams and sponsors.
• Demonstrated leadership ability, including experience leading study teams or overseeing sponsor-specific programs.

Precision for Medicine is committed to fostering a supportive and collaborative work environment where our employees can thrive professionally. Joining our team offers several advantages:

• Fully remote work flexibility, allowing for a healthy work-life balance across multiple European locations.
• The opportunity to work on diverse and innovative clinical trials in cutting-edge therapeutic areas like oncology and rare diseases.
• A clear career progression path with opportunities for continued learning, advanced certification support, and leadership exposure.
• Competitive compensation packages tailored to the local market and your specific experience level.
• A collaborative global culture that values diversity, innovation, and the shared goal of improving patient lives through precision medicine.

Required Skills