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Sr. Clinical Research Associate
Eingestellt von Real Staffing Group aus Frankfurt am Main
Projektbeschreibung
Roles:
* Monitor and track patients in study sites and treatment outcome collection programs
* Ensure adequate documentation and proper implementation of written protocols
* Assist in writing and developing clinical protocols, data tracking forms, informed consent documents, and clinical report forms. Secure approvals from regulatory and/or legal as needed for the program
* Provide technical assistance to study sites regarding the conduct of clinical research
Track data report forms, reports, and documents necessary for completion of clinical study, both in-house and from participating study sites
* Ensure that milestone payments are made according to protocol and budget timeline
* Comply with all regulatory and safety policies, practices and procedures. Report all unsafe activities to supervisor and/or Human Resources
Requirements:
* Bachelor of Science, or equivalent experience (MS preferred)
* 5-6 years of experience as a Clinical Research Associate
* Experienced in desiging and running pre-market and post-market clinical studies for medical device companies
To find out more about Real please visit www.realstaffing.com
Projektdetails
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Einsatzort:
San Jose, California, 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:
Sonstiges