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Senior Clinical Data Manager
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Maidenhead, Windsor and Maidenhead, United Kingdom Lifelancer Full timeSenior Clinical Data ManagerFortrea, a leading global contract research organization, is seeking a highly skilled Senior Clinical Data Manager to join our Global Clinical Development department. As a key member of our team, you will be responsible for leading data management activities across late-phase studies, collaborating with cross-functional teams, and...
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Senior Clinical Data Manager
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Senior Clinical Data Manager
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Senior Clinical Data Manager
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Senior Clinical Data Manager
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Maidenhead, Windsor and Maidenhead, United Kingdom Pharmiweb Full timeJob Title: Senior Clinical Data ManagerAbout the Role:As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across...
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Maidenhead, Windsor and Maidenhead, United Kingdom Fortrea Full timeJob SummaryFortrea is seeking a highly skilled Senior Clinical Data Manager to join our team in EMEA. As a Senior Clinical Data Manager, you will be responsible for leading complex oncology clinical trials and providing CDM leadership for one or more assigned projects or indications. You will demonstrate leadership and operational expertise in the strategic...
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Senior Clinical Data Manager
2 months ago
Fortrea is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.
Job SummaryWe are seeking a highly motivated and experienced Senior Clinical Data Manager to join our team. As a Senior Clinical Data Manager, you will be responsible for the full cycle of Clinical Data Management queries, from being in full leadership of your own studies and being the main point of contact with the client, to the most hands-on tasks such as creating eCRFs, cleaning data, and performing independently set-up to close-outs duties.
Key Responsibilities- Provides CDM leadership for one or more assigned projects or indications dependent on size and scale of the project.
- Demonstrates leadership and operational expertise in the strategic planning and delivery of CDM deliverables at program and/or project level.
- Communicates and negotiates effectively with all other Program level team members.
- Provides oversight and expertise of external service providers or in-house teams to deliver quality data with compliance to study model procedures and standards.
- Responsible for proactive risk management and issue resolution/escalation connected to Clinical Data Management improvement or technology.
- University/college degree (life science, pharmacy, or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution.
- Experience in leading complex oncology clinical trials.
- Extensive experience in clinical data management and experience leading studies in a CRO/Pharma setting.
- In-depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.
- Office based or home based anywhere in Europe.
- Rewarding and meaningful work in an established, diverse, highly profitable, and respected global company.
- Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances, etc.
- A genuine work-life balance.
- Flexibility in working hours.
- A thorough onboarding with support from your personal mentor.
- A permanent employment contract with Fortrea Drug Development and a rewarding career progression.
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.