CLINICAL DATA MANAGEMENT SPECIALIST

at  KCR Placement

KCR Placement is a full-service functional sourcing and recruitment provider. We specialize in high-speed and high-quality talent sourcing for the CRO, Pharmaceutical, Biotech and Medical Device industries across Europe.
Our employees are KCR Placement’s most crucial asset. We commit to placing our candidates at the center of all we do and prepare them for long-term career development and success with competitive benefits and vibrant work environment.
The KCR Placement team is supported by a specialized referral network of expert professionals and is dedicated to providing sourcing services and client support from job requisition to job offer.
We are looking for flexible, communicative candidates with analytical mind to join our KCR Placement Data Management Team. This position is dedicated to one Sponsor and ensures possibility of dynamic career within our Client’s projects, including assignments in Experts Teams supporting data standardization in clinical trials.

REQUIREMENTS:

• University degree in the field of biotechnology, medical chemistry, pharmacy, biology, veterinary medicine, medical analytics, medicine, life science, biophysics, biochemistry, bioinformatics, biomedical engineering;
• Very good written and spoken English;
• Computer literacy and ease of learning new computer systems and applications;
• High level of organizational and time management skills;
• Eager to follow the procedures;
• Analytical skills and problem-solving competencies;
• Adaptability in dynamic, fast-changing work environment;
• Readiness for smooth cooperation in the team, based on high level communication skills and mutual respect;
• Experience in the field of clinical trials, especially directly in the field of clinical data management would be beneficial.

• Entering clinical trials data into the system;
• Quality control of the entered data in accordance with received guidelines, ensuring consistency and compliance with formal requirements;
• Generating inquiries to Investigators in order to clarify inconsistencies and verify received responses;
• Identifying missing data;
• Collaboration with international clinical research teams;
• Participation in the processes at different stages of clinical trials e.g. start-up, database lock.