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Parexel
Parexel Initiation Clinical Research Associate Recruitment 2026: Apply Online
Initiation Clinical Research Associate – iCRA
Experience Required
Experienced / Professional
Salary / Package
Competitive
Work Mode
Remote
Openings
1
Job Overview
- As an Initiation Clinical Research Associate (iCRA) at Parexel, you will lead and execute all study start-up, pre-SIV, activation, and protocol amendment activities.
- Serve as the primary contact for assigned sites, successfully managing regulatory submissions, site readiness, and document quality.
- Collaborate with investigators and site staff to build strong, enduring professional relationships while tracking activation strategies and timelines.
- Ensure compliance with all sponsor requirements, local regulations, and company standard operating procedures (SOPs).
- Maintain rigorous documentation standards across CTMS, eTMF, and TMF systems to achieve First Time Quality (FTQ).
- Identify, resolve, and escalate potential site issues or activation risks proactively.
- Work within a global, matrixed, and multicultural environment supporting life-saving clinical research trials.
Key Job Details
| Company Name | Parexel |
| Job Role | Initiation Clinical Research Associate – iCRA |
| Experience | Experienced / Professional |
| Salary Range | Competitive |
| Job Type | Full-time |
| Work Mode | Remote |
| Openings | 1 |
| Job Location | Brazil (Remote) |
Key Responsibilities
- Manage site start-up activities from feasibility and qualification through activation.
- Build and maintain strong relationships with investigators and site staff.
- Prepare, review, negotiate, and execute regulatory and site documents including CDAs and ICFs.
- Coordinate submissions and approvals with IRBs/IECs, Ministries of Health, and Regulatory Authorities.
- Maintain high-quality documentation in CTMS, eTMF, and TMF systems.
- Ensure sites remain audit- and inspection-ready throughout the study lifecycle.
Requirements & Qualifications
- Strong background in clinical research and study start-up processes.
- Excellent problem-solving, communication, and stakeholder management skills.
- Ability to work independently and prioritize multiple tasks in dynamic environments.
- Proficiency in CTMS, eTMF, TMF, and Microsoft Office tools.
- Fluency in English (oral and written).
Required Skills
- Communication
- Detail-oriented
- Flexibility
- Organizational Skills
- Problem-solving
- Self-starter
About Parexel
Parexel is a leading global clinical research organization (CRO) focused on helping pharmaceutical, biotechnology, and medical device clients accelerate the delivery of innovative treatments to patients worldwide with heart and dedication.
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Frequently Asked Questions
Q: What qualifications are required for the iCRA position?
A: A Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a health-related field is preferred along with relevant clinical research experience.
Q: Is this a remote work opportunity?
A: Yes, this position is offered as a remote-based role in Brazil with flexible working options.
Q: What are the primary responsibilities of an iCRA?
A: An iCRA is responsible for leading study start-up, pre-SIV, site activation, regulatory submissions, and maintaining documentation quality.
Q: How do I apply for this vacancy?
A: You can apply directly online by navigating to the application link provided on JobsCheck.
Q: Does Parexel offer career growth opportunities?
A: Yes, Parexel provides structured professional development programs, mentorship, and clear career paths within clinical operations.
Disclaimer: This job post is prepared by collecting data from the official career page of Parexel. We are not direct recruiters or representatives. Candidates should carefully review the requirements and policies on the company’s portal before initiating an application.