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⏳ Last Date to Apply: As soon as possible
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Parexel
Parexel Clinical Trial Manager Recruitment 2026: Apply Online
Clinical Trial Manager – Spain – FSP
Experience Required
5 or more years of industry experience in clinical trial project management
Salary / Package
Competitive Premium Salary with Comprehensive Benefits
Work Mode
Remote / Home-based
Openings
1
Job Overview
- Manage external vendors and contract research organizations efficiently to ensure execution of clinical trials.
- Prepare study documents including Monitoring Manuals, Study Operations Manuals, and Source Data Verification Plans.
- Coordinate study materials design such as case report forms (CRFs), patient diaries, and source documents.
- Support protocol development, study report completion, and coordinate study supplies.
- Assure regulatory compliance with FDA, ICH guidelines, and sponsor standard operating procedures (SOPs).
- Monitor activities at clinical study sites, provide guidance to CRAs, and review site reports.
Key Job Details
| Company Name | Parexel |
| Job Role | Clinical Trial Manager – Spain – FSP |
| Experience | 5 or more years of industry experience in clinical trial project management |
| Salary Range | Competitive Premium Salary with Comprehensive Benefits |
| Job Type | Full-Time |
| Work Mode | Remote / Home-based |
| Openings | 1 |
| Job Location | Spain (Remote / Home-based) |
Key Responsibilities
- Oversee all aspects of clinical trials from initiation to closeout within budget and timelines.
- Identify and resolve trial execution issues promptly to maintain study integrity.
- Manage multiple tasks, deadlines, and priorities in complex clinical trial environments.
- Convey clear information and expectations to cross-functional teams, investigators, and stakeholders.
- Ensure Trial Master File is current and properly maintained.
Requirements & Qualifications
- 5+ years of industry experience in clinical trial project management across international trials.
- Proven background as a CRA or clinical trial manager within pharmaceutical, biotech, or CRO sectors.
- Demonstrated working knowledge of GCP, ICH guidelines, and regulatory requirements.
- Proficiency with MS Office applications (Word, Excel, PowerPoint, Outlook).
- Excellent oral and written communication skills with strong organizational abilities.
Required Skills
- Clinical Project Management
- Vendor & CRO Management
- Regulatory Compliance (GCP/ICH)
- Data Management & Query Resolution
- Matrix Leadership & Communication
About Parexel
Parexel is a leading global clinical research organization (CRO) dedicated to accelerating the development of innovative new medicines and therapies to improve patient health worldwide through scientific excellence, innovation, and commitment.
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Frequently Asked Questions
Q: Is this a remote work opportunity?
A: Yes, this position is a home-based role located in Spain.
Q: What is the educational requirement for this role?
A: A Bachelor’s degree, nursing degree, or equivalent is required, with a background in science preferred.
Q: How many years of experience are needed?
A: Candidates must have 5 or more years of industry experience in clinical trial project management.
Q: What benefits are offered with this position?
A: Parexel offers a premium salary, attractive benefits, a comprehensive medical care plan (health, dental, and vision), and life assurance.
Q: How can I submit my application?
A: Applications can be submitted online through the official Parexel career portal using the direct apply link provided.
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.