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Parexel
Parexel Study Start-Up Specialist Site Activation Partner – FSP Recruitment 2026: Apply Online
Study Start-Up Specialist / Site Activation Partner – FSP
Experience Required
Minimum 2 years of relevant experience in a clinical trials environment or pharmaceutical industry
Salary / Package
Competitive & Industry Standard
Work Mode
Remote / Hybrid
Openings
1
Job Overview
Parexel is seeking a dedicated and detail-oriented Study Start-Up Specialist / Site Activation Partner – FSP to join our global team in Ontario, Canada. In this role, you will play an essential part in accelerating new medical treatments to patients by ensuring efficient clinical trial start-ups and flawless regulatory compliance.
- Lead and coordinate start-up to close-out operational activities for assigned clinical trials and investigator sites.
- Compile high-quality Investigator Initiation Packages (IIP) and manage essential study documentation.
- Liaise with local regulatory bodies and ethics committees to facilitate parallel submissions and approvals.
- Maintain clinical trial management systems accurately to track site performance, timelines, and compliance metrics.
- Identify potential site roadblocks early and implement prompt resolution strategies.
Key Job Details
| Company Name | Parexel |
| Job Role | Study Start-Up Specialist / Site Activation Partner – FSP |
| Experience | Minimum 2 years of relevant experience in a clinical trials environment or pharmaceutical industry |
| Salary Range | Competitive & Industry Standard |
| Job Type | Full Time |
| Work Mode | Remote / Hybrid |
| Openings | 1 |
| Job Location | Canada – Ontario (Remote) |
Key Responsibilities
- Coordinate and manage investigator initiation documents to achieve rapid site activation approval.
- Resolve site-level operational concerns and escalate critical issues appropriately.
- Collaborate with internal country regulatory groups and external sponsors seamlessly.
- Update clinical trial tracking databases to reflect accurate compliance and milestone data.
- Ensure all activities strictly adhere to ICH/GCP guidelines, FDA rules, and local legal standards.
Requirements & Qualifications
- Proven experience working within clinical trials, pharmaceutical companies, or Contract Research Organizations (CROs).
- Solid understanding of clinical trial methodologies, ICH/GCP guidelines, and regulatory requirements.
- Fluent in English with exceptional written and verbal communication skills.
- Strong interpersonal traits including being a self-starter, detail-oriented, and an effective problem-solver.
Required Skills
- Clinical Trial Management
- Regulatory Compliance
- Document Control & Management
- Problem-Solving & Critical Thinking
- Cross-functional Communication
- Time Management & Organization
About Parexel
Parexel is a leading global Clinical Research Organization (CRO) providing comprehensive drug development services to biopharmaceutical and medical device companies. We combine clinical expertise with advanced technology and a patient-first culture to accelerate the delivery of life-changing treatments to patients worldwide.
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Frequently Asked Questions
Q: What does a Study Start-Up Specialist do at Parexel?
A: They manage operational activities from start-up to close-out, coordinate essential documents for site initiation, and ensure regulatory compliance.
Q: What educational background is required?
A: A school diploma with equivalent experience is required, though a Bachelor’s degree in Life Sciences is preferred.
Q: How many years of experience are needed?
A: At least 2 years of relevant experience in a clinical trials environment or pharmaceutical industry is required.
Q: Is this a remote position?
A: Yes, this position offers flexible remote working arrangements based in Ontario, Canada.
Q: How can I submit my application?
A: You can apply online directly through the official Parexel Workday career link provided on JobsCheck.
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.