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Clinical Research Associate Job
Eingestellt von Yoh
Gesuchte Skills: Support, Client
Projektbeschreibung
WHAT YOU'LL BE DOING:
- Review of draft SAE case narratives and other narratives for events of special interest for understandability, consistency and medical correctness (~200 narratives)
- Review and interpretation of concomitant medication listings as provided from verbatim in case report forms (~750 records)
- Assignment of generic drug name (may be provided in listing as country specific brand name)
- Assignment of dosing regimen (may be provided in medical short hand)
- Clinical Review of patient profiles and data listings to check for completeness, discrepancies and protocol deviations
- Support clinical data review and resolution of queries
- Support clinical team activities to review draft statistical outputs for format and completeness
WHAT YOU NEED TO BRING TO THE TABLE:
- MD or non-MD clinical scientist with several (5) years experience with cardiovascular trials (heart failure trial experience would be most relevant)
- Experience in contributing to and reviewing clinical study reports.
- Demonstrated knowledge of cardiovascular medicine and medications sufficient to accomplish the tasks shown above.
- Experience with morbidity and mortality trials (M&M trials) valued
- Excellent oral and written communication skills
- Experience with writing protocols, clinical study reports, or manuscripts
- Demonstrated experience reviewing and interpreting complicated clinical data sets: this is a complicated trial with over 700 data tables anticipated
- Strong analytical skills- ability to review and understand complex data sets and make recommendations/proposals for resolving data issues
OPPORTUNITY IS CALLING, APPLY NOW!
RECRUITER: Krista Leach
J2W: CLINICAL
MONJOBJ2WMIDATL
Ref:
SFSF: LS
Projektdetails
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Einsatzort:
East Hanover, 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