What are the responsibilities and job description for the Contract CRA position at Actalent?
Description:
RESPONSIBILITIES:
Write site visit trip reports
Compile and ensure completeness of regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB / IEC study approval, informed consent, etc.)
Coordinate study material (e.g. CRFs, manuals) shipment and receipt by study site
Document site visit findings via written reports
Review study subject safety information and informed consent
Conduct source document verification for compliance, patient safety, and veracity of data
Review CRFs using paper or electronic data capture systems and assist sites with data query resolution
Maintain regular communication with sites
Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
Skills:
CRA, Clinical Research Associate, site, monitor, visits
Top Skills Details:
CRA,Clinical Research Associate,site, monitor, visits
Additional Skills & Qualifications:
REQUIREMENTS: Requires a bachelor degree or a two-year nursing degree A minimum of 2 years of field monitoring experience required CNS experience required Acute Pain, Alzheimers or ALS/Parkinsons preferred Willingness to travel per Region required
Experience Level:
Expert Level
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Responsibilities:
Description:RESPONSIBILITIES:Write site visit trip reportsCompile and ensure completeness of regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB / IEC study approval, informed consent, etc.)Coordinate study material (e.g. CRFs, manuals) shipment and receipt by study siteDocument site visit findings via written reportsReview study subject safety information and informed consentConduct source document verification for compliance, patient safety, and veracity of dataReview CRFs using paper or electronic data capture systems and assist sites with data query resolutionMaintain regular communication with sitesPerform other duties as assigned.Salary : $70 - $90
