What are the responsibilities and job description for the Clinical Research Associate (1099 Contract) position at Actalent?
Clinical Research Associates
Remote with aprox. up to 30% travel
Additional Skills & Qualifications:
- This is a 1099 contract/consulting opportunity
- Low travel (aprox. up to 30%)
- Central and East Coast location highly preferred
- 4 years of CRA monitoring experience required
- Prior experience with Covid Studies is a huge plus
- 4 year degree from accredited institution
Description:
- Participate in site selection and in training site personnel regarding the trial; perform site monitoring duties and follow-up to ensure identified deficiencies are corrected; travel as required to accomplish responsibilities.
- Participate in the development of protocols, informed consent forms, case report forms (CRFS) and instructions, site selection materials, procedure/in service manuals, project newsletter, project specific standard operating procedures, and other monitoring tools for the clinical trial. Follow established guidelines in the collection of clinical data and/or administration of clinical trials.
- Assist in assessing the suitability of potential investigative sites through telephone screening interviews, regulatory document review and disseminating clinical trial information; conduct site qualification visits to determine adequacy of facilities and staff, patient recruitment and retention potential, ability to comply with regulatory requirements, and overall interest and commitment of principal investigator to conduct and complete the planned clinical study.
- Conduct site initiation visits as needed for the purpose of training site personnel about the protocol, study procedures, patient recruitment and retention requirements, regulatory requirements, case report form completion and retention requirements, drug accountability procedures, and serious adverse events (SAES) , reporting procedures, and overall management.
- Conduct monitoring visits to assure the integrity of clinical data with respect to accuracy, accountability, documentation, and methods or procedures through review of CRFS, source documents, medical records, and regulatory documents; provide feedback to assigned sites and information regarding detected deficiencies and corrective action needed. Follow-up with sites until deficiencies are resolved. Perform other related duties incidental to the work described herein.
Experience Level:
Intermediate Level
Skills:
CRA, Clinical Research Associate, sites, visits, monitor, Covid-19, Infectious Disease
Top Skills Details:
CRA, Clinical Research Associate, sites, visits, monitor
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.
Salary : $75 - $85
