Senior Clinical Data Manager - sponsor dedicated - oncology — Fortrea | Joboostr

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Senior Clinical Data Manager - sponsor dedicated - oncology — Fortrea | Joboostr

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Senior Clinical Data Manager - sponsor dedicated - oncology

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Remotepřed 3 dny

Mám zájem Přizpůsobit životopis

O pozici

Senior Clinical Data Manager – FSP / oncology experience The Senior Clinical Data Manager role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor.

Co budeš dělat

Provides CDM leadership for one or more assigned projects or indications dependent on size and scale of the project.
Lead studies including (but not limited to) a combination of healthy volunteer and patient populations, multi-site, complex protocol design, strong client management required or reduced timelines.
Demonstrates leadership and operational expertise in the strategic planning and delivery of CDM deliverables at program and/or project level.
Management and oversight of vendor contracts, resourcing and budget management and oversight of vendor performance for assigned programs, and projects
Communicates and negotiates effectively with all other Program level team members.
Primary point of contact for Clinical Data Management (CDM)
Provide 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
Develops an understanding of CDASH and SDTM or other recognized industry standards and impact to programming team to ensure consistency of program level standards.

Koho hledáme

University/college degree (life science, pharmacy or related subject preferred)
8 years of combined early or late-stage DM experience with minimum 2 years of direct sponsor management and at least 2 years technical mentoring experience.
Extensive experience in clinical data management and experience leading studies in a CRO/Pharma setting.
Understanding of RECIST criteria.
Excellent oral and written communication and presentation skills.
In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.
Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.

Benefity

Office based or home based anywhere in the listed countries
Exposure to high profile global studies with 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

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