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Clinical Research Associate Job
Eingestellt von Yoh
Gesuchte Skills: Client
Projektbeschreibung
WHAT YOU'LL BE DOING:
- Assist in the management of the day to day operations of clinical trials including coordination and oversight of all CRO/clinical site/vendor activities
- Liaison between Clinical Operations Manager and CRO, manage scopes of work/budgets/invoice payments.
- Assist in the management of the Trial Master File (submit documents, reconciliation, QC)
- Participate in development of protocol, case report form, CRF guidelines and other study documents.
- Prepare and/or review regulatory documents (eg ICF), contracts, requests for proposal.
- Ensure the training of CROs/investigators on protocol, regulatory, and data issues.
- Reviews and approves monitoring reports and ensures tracking of ongoing site issues.
WHAT YOU NEED TO BRING TO THE TABLE:
- Bachelors degree in relevant scientific discipline
- Three to five (3-5) years experience in pharmaceutical industry.
- Oncology Experience Highly Preferred
OPPORTUNITY IS CALLING, APPLY NOW!
RECRUITER: Krista Leach
Yoh, a DayPROF
MONJOBJ2WMIDATL
Ref:
SFSF: LS
Projektdetails
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Einsatzort:
Woodcliff Lake, Vereinigte Staaten
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
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Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung