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Clinical Trials Assistant I Job
Eingestellt von Yoh
Gesuchte Skills: Client
Projektbeschreibung
THE BIG PICTURE - TOP SKILLS YOU SHOULD POSSESS:
- Pharmaceutical
- Microsoft Office
- Clinical Trials
WHAT YOU'LL BE DOING:
- Assist Clinical Trial Management to ensure accurate, timely, and coordinated availability of clinical trial materials and documents.
- Mentor and assist with training of incoming CTAs. Assist with process improvement efforts.
- Enter and maintain current data in clinical systems (ie, enrollment as requested, EDC access maintenance, etc.).
- Coordinate printing of Investigator Study File (ISF) and other study materials and distribution to the sites at study start and as needed during the study.
- Review proof copy of study material and coordinate correction of errors prior to printing complete package.
- Assist with preparation of training material.
- Assist with compliance review of clinical documentation as requested by CTDM.
- Coordinate test article reconciliation and resolution of issues with LCSM.
- Assist Site Development as requested by manager.
- No delays in study start-up cycle time.
- Integrity and quality of printed materials, study documents, and training materials.
- Standard and consistent processes and procedures across studies and TA's.
WHAT YOU NEED TO BRING TO THE TABLE:
- Associates degree or certification in medical field with 2 years experience.
- Bachelor's degree in an appropriate discipline and at least 2 years experience related to clinical research.
- Advanced skills in Microsoft Office to include Word, Excel, Powerpoint.
- Excellent oral and written communication skills.
WHAT ARE YOU WAITING FOR? APPLY NOW!
RECRUITER:Corrin Pyle
Yoh, a DayJ2W: SCIENTIFIC; MONJOB
TAXTERM: CON_W2J2WSWSCI
Ref:
SFSF: LS
Projektdetails
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Einsatzort:
Fort Worth, 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