Oferta pracy - KCR Placement
KCR Placement is a highly specialized provider of ‘fit for purpose’ full-spectrum resourcing solutions in Life Sciences industries. The company specializes in finding the right talents for pharma, biotech, medical device companies and contract research organizations (CROs) across Europe. Founded as a sister company of KCR, an international CRO, we are supported by a great referral network of trusted professionals and provide full cycle recruitment services from job requisition to job offer. Our core services include Permanent Placement, Temporary Placement, Contract Placement, Executive Placement and Outplacement. KCR Placement has its offices in Berlin, Germany, Warsaw, Poland and Prague, Czech Republic. For more information please visit www.kcrplacement.com. We are currently looking for suitable candidates that would be dedicated to the projects of one of the top 5 big pharma companies in the position of:
Clinical Data Management Specialist
Duties:
Verifying and entering clinical trials data into the system
Quality control of the entered data, ensuring consistency and compliance with formal requirements
Generating inquiries to Investigators in order to clarify irregularities and verify received responses
Identifying missing or incorrect data (in accordance with received guidelines)
The role of the Project Coordinator: communication with Clinical Trial Monitors and foreign Clinical Research Data Management Centers, ensuring the implementation of individual stages of the project according to the established schedule and timelines
Collaboration with international clinical research teams
Participation in the database closure process at the final stage of the study
Dynamic career within our Client’s projects, including assignments in Experts Teams supporting data standardization and optimization 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 and sciences
Experience in the field of clinical trials, especially directly in the field of clinical data management would be beneficial (we offer full training support for unexperienced candidates)
Very good written and spoken English
Computer literacy and ease of learning new computer systems and applications
High level of organizational skills, ability to follow procedures, good time management and ability to set priorities
Analytical skills and problem-solving competencies
Ability to work in a team with high level of communication skills
Ability to go extra mile and create friendly working atmosphere based on mutual respect
Open for candidates across Poland – company support in relocation to Warsaw
Stable employment contract
Hybrid working model
Entering business growth opportunities, training and mentoring programs related to clinical trials and soft skills
Great atmosphere within innovative team and empowering environment to share ideas
Peer Buddy Mentor introducing you to the organization
Medical care package, sport card and other attractive benefits
