Contract CRA

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