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TPI Global (formerly Tech Providers, Inc.)
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Clinical Research Associate
Posted: 01/24/2024
2024-01-24
2024-04-04
Job Number: 21161150
Job Description
Job Title: Clinical Research Associate
Location: East Coast (Candidate on East Coast preferred)
Travel: Heavy travel required (80%)
Contract Duration: Through June 2024 (Project approved for 24 months - likely to extend or convert)
Brief Details:
This role is on a contract basis through June 2024, with the project approved for 24 months and a strong likelihood of extension or conversion. The candidate must be prepared for heavy travel, possess excellent communication skills for remote consenting, and demonstrate proficiency in various aspects of clinical trial management.
Trial Focus: Respiratory Trial/Phase 4 Trial
Note: Qualified candidates are encouraged to apply, especially those with a strong background in respiratory trials, extensive CRA experience, and a track record of success in decentralized trial settings.
Project Overview:
Responsibilities:
Skills:
Location: East Coast (Candidate on East Coast preferred)
Travel: Heavy travel required (80%)
Contract Duration: Through June 2024 (Project approved for 24 months - likely to extend or convert)
Brief Details:
This role is on a contract basis through June 2024, with the project approved for 24 months and a strong likelihood of extension or conversion. The candidate must be prepared for heavy travel, possess excellent communication skills for remote consenting, and demonstrate proficiency in various aspects of clinical trial management.
Trial Focus: Respiratory Trial/Phase 4 Trial
Note: Qualified candidates are encouraged to apply, especially those with a strong background in respiratory trials, extensive CRA experience, and a track record of success in decentralized trial settings.
Project Overview:
- The Clinical Research Associate will be an integral part of a Respiratory Trial/Phase 4 Trial, responsible for enrolling 700 patients, averaging 16 patients per week. The trial involves a high volume of patients, and the ideal candidate will excel in consenting patients over the phone and via Zoom, demonstrating comfort in virtual environments.
Responsibilities:
- Conduct heavy travel on a weekly basis to various trial sites.
- Consenting patients over the phone and via Zoom, managing a high volume efficiently.
- Work on different stages of the clinical trial, including initiation, maintenance, and close-out.
Skills:
- Therapeutic experience in respiratory trials is highly beneficial.
- 5+ years of experience as a Clinical Research Associate, with a proven track record in conducting different stages of clinical trials.
- CRA Certification is preferred.
- Experience with remote monitoring and E-consent.
- Proficient in working with decentralized trials and monitoring.
- Familiarity with Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), and electronic Trial Master File (eTMF).
- Prior experience in Contract Research Organization (CRO) settings is a plus.
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