Posted 3 months ago
Clinical Trial Associate
AI Summary
A Clinical Trial Associate supports clinical operations project teams by assisting with pre- and post-approval clinical trial processes, including quality review and document preparation under general supervision.
About this role
Clinical Trial Associate
IRI believes in commitment, integrity and strategic workforce solutions.
Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.
We’ve stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.
Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients’ success.
Job Title: Clinical Trial Associate
Location: Lexington, MA
Duration: 3 Months +
Job Summary:
Responsible for assisting and providing support to the members of the clinical operations project team (i.e. Clinical Project Managers, Associate Directors, or Directors), in order to facilitate the management of pre- and post-approval clinical trial processes including quality review and document prep. The CTA performs work within established protocols under general supervision.
Responsibilities:
• Main priority is candidate is competent and able to do this role, and start ASAP.
• Candidate needs to be able to jump in and do work well.
• Candidate will be working on documentation review in QC.
• Candidate must understand clinical trial process and documentation.
• Must have SOME experience in clinical trial process and documentation.
• Willing to see new graduates as long as they have some experience.
Qualifications
Must have SOME experience in clinical trial process and documentation.
• Willing to see new graduates as long as they have some experience.
Additional Information
Amrit Singh
Clinical Recruiter
Integrated Resources, Inc.
IT REHAB CLINICAL NURSING
Tel: (732) 429 1634 (Direct)
Ext: (732) 549 2030 x (212)
Fax: (732) 549 5549
http://www.irionline.com
Inc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012, 2013 & 2014 (8th Year)
Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70
https://www.linkedin.com/company/46970?trk=prof-exp-company-name
Skills
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