Remote Clinical Research Job at Parexel | Apply Now
A Parexel Clinical Research Job opportunity has arisen for aspiring Clinical Research Associates. This role, available remotely in Brazil, Colombia, and Mexico, invites qualified candidates to contribute to the critical work of advancing healthcare solutions. Applications are encouraged from individuals eager to make a difference in clinical research.
- Position: Initiation Clinical Research Associate – iCRA
- Primary Location: Brazil, Remote
- Additional Locations: Colombia, Remote; Mexico, Remote
About Parexel
Parexel is a leading global biopharmaceutical services organization that provides a comprehensive range of services to the pharmaceutical, biotechnology, and medical device industries. With a commitment to advancing healthcare and improving patient outcomes, Parexel operates in various therapeutic areas and supports clients in bringing innovative treatments to market efficiently and safely.
Job Description
This Parexel Clinical Research Job involves leading and executing all study start-up, pre-SIV, activation, and protocol amendment activities: from site identification through site activation and maintenance. Acting as the primary contact for assigned sites, the Initiation Clinical Research Associate (iCRA) manages regulatory submissions, site readiness, document quality, and activation timelines while ensuring compliance with sponsor, regulatory, and company requirements.
Eligibility Criteria for Clinical Research Job
- Bachelor’s degree in Life Sciences, or other related field (or equivalent experience) is preferred.
- Excellent problem-solving, communication, presentation, and stakeholder management skills.
- Ability to work independently, prioritize multiple tasks, and make decisions in ambiguous situations.
- Strong knowledge of CTMS, eTMF, TMF, and Microsoft Office tools.
- Experience working in global, matrix, and multicultural environments.
Key Responsibilities for the Clinical Research Job
- Managing site start-up activities from feasibility and qualification through activation.
- Building strong relationships with investigators and site staff.
- Preparing, reviewing, negotiating, and executing regulatory and site documents, including CDAs, ICFs, translations, and amendments.
- Coordinating submissions and approvals with IRBs/IECs, Ministries of Health, and Regulatory Authorities.
- Developing and tracking activation strategies, timelines, and regulatory plans.
- Maintaining high-quality documentation in CTMS, eTMF, and TMF systems, ensuring First Time Quality (FTQ).
- Identifying, resolving, or escalating site issues and risks related to activation, recruitment, compliance, training, and data quality.
- Ensuring sites remain audit- and inspection-ready throughout the study lifecycle.
- Maintaining compliance with ICH-GCP guidelines, local regulations, sponsor requirements, and Parexel SOPs.
This Parexel Clinical Research Job offers a significant opportunity for Clinical Research Associates to engage in meaningful work that impacts patient care. Qualified candidates are encouraged to apply before the deadline to be part of a dedicated team committed to excellence in clinical research.
