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Clinical Trial Manager Job
Eingestellt von Yoh
Gesuchte Skills: Support, Client
Projektbeschreibung
WHAT YOU'LL BE DOING:
- Provides support and/or leadership to one or more global Study Teams within an early development program(s) (ie phase I and II trials).
- The cCTM is accountable for activities ensuring high quality deliverables are within budget and timelines.
- Primary Accountabilities and Responsibilities:
- Support cross-functional Study Team within Clinical Operations with minimal oversight from the Sr. CTM and/or CPL
- Responsible for Clinical Operations deliverables to achieve study objectives and milestones within timelines and budget
- Responsible for vendor selection and management including CRO, IVRS, central lab and imaging vendor
- Provide input to the study budget and is responsible for managing assigned vendor budget(s)
- Under the leadership of the Sr. CTM, takes responsibility for agreed operational aspects (eg, vendor management, drug supply management)
- Identify and track timelines, milestones, critical study activities, issues and budget and provide regular updates to the Study Team and CPL as appropriate
- Partner with CPL to develop and/or present at project teams and management review bodies
- Conduct protocol and site feasibility assessments
- Ensure relevant functional groups provide input to and participate in developing and finalizing Study Team level documents and meet Study Team level deliverables within timelines
- Accountable for Clinical Operations deliverables to achieve study objectives and milestones within timelines and budgets
- Provide input to the program budget and is accountable for managing overall study budget where assigned
- Delegate and oversee study activities assigned to Clinical Operations Study Team as applicable
WHAT YOU NEED TO BRING TO THE TABLE:
- Bachelors degree or equivalent undergraduate degree (scientific or healthcare discipline preferred)
- Five (5+) years direct industry study management experience in clinical and drug development
- Working knowledge of international regulatory and ICH GCP guidelines
- Experienced in clinical trial management
- Experience in planning, risk mitigation strategies, trial budgets, site selection, clinical supplies management, conduct and monitoring of clinical studies
- Familiar with global trial requirements
- Demonstrated creativity and innovation to support projects and initiatives
- Excellent planning and organizational skills
- Flexible and solution focused
- High level of initiative and ability to work independently
OPPORTUNITY IS CALLING, APPLY NOW!
RECRUITER: Krista Leach
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.
J2W: CLINICAL
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Ref:
SFSF: LS
Projektdetails
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Einsatzort:
South San Francisco, Vereinigte Staaten
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Sonstiges