Apply for Site Start Up EUCTR I job at Parexel Hyderabad. Check eligibility, responsibilities, salary details, and application process now.
Introduction
If you are looking to build a strong career in clinical research and regulatory operations, this opportunity can be a great step forward. The Site Start Up EUCTR I Job at Parexel offers hands-on exposure to global clinical trial processes, especially within European regulatory frameworks. Candidates with a background in life sciences and initial experience in clinical trials can benefit from this role by gaining industry-relevant expertise and career growth.
Job Overview
| Job Details | Information |
|---|---|
| Job Title | Site Start Up EUCTR I |
| Company Name | Parexel |
| Location | Hyderabad, India |
| Employment Type | Full-Time |
| Department | Clinical Research / Regulatory Affairs |
| Experience Required | 1–2 Years |
| Education | Bachelor’s Degree |
| Salary | As per company norms |
Company Overview
Parexel is a globally recognized clinical research organization (CRO) dedicated to improving patient health through innovative clinical development solutions. The company supports pharmaceutical, biotechnology, and medical device industries by offering services ranging from clinical trials to regulatory consulting. Known for its patient-first approach, Parexel emphasizes quality, compliance, and innovation in every project.
Job Location & Employment Type
- Location: Hyderabad, India
- Job Type: Full-Time
- Work Mode: Office-based (may include some travel requirements)
Open Positions / Department Details
This opening is part of the Clinical Trial Start-Up and Regulatory Operations team, focusing on European Union Clinical Trial Regulation (EUCTR) submissions and compliance. The role involves collaboration with multiple departments such as Clinical Operations, Regulatory Affairs, and Clinical Transparency teams.
Key Roles & Responsibilities
The Site Start Up EUCTR I Job at Parexel involves a mix of regulatory coordination, documentation, and project support tasks. Key responsibilities include:
- Supporting the planning and submission of EUCTR-related clinical trial applications
- Coordinating with clinical trial teams to define study timelines and country strategies
- Preparing and managing Part-II Clinical Trial Applications (CTA) for EU countries
- Identifying participating countries and maintaining records in CTIS systems
- Collecting and organizing country-specific regulatory documents
- Uploading required documentation into clinical trial databases
- Collaborating with stakeholders for document redaction and transparency requirements
- Tracking study milestones such as enrollment, completion, and trial start dates
- Ensuring compliance with ICH-GCP, EUCTR, and IVDR guidelines
- Handling Requests for Information (RFIs) and coordinating responses
- Maintaining proper documentation and archiving as per regulatory standards
- Managing investigator and site-related data throughout the study lifecycle
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field
Experience
- 1–2 years of experience in clinical research or regulatory affairs
- Exposure to clinical trial start-up activities is preferred
Skills Required
- Knowledge of clinical trial processes and EU regulations
- Understanding of ICH-GCP and regulatory compliance standards
- Basic knowledge of CTMS, TMF, and clinical databases
- Strong communication and coordination skills
- Ability to manage multiple tasks and meet deadlines
- Data-driven mindset for planning and execution
- Good proficiency in MS Office tools (Word, Excel, PowerPoint)
- Team collaboration and problem-solving skills
Salary & Benefits
- Salary: As per company norms
- Additional benefits may include:
- Health insurance
- Performance-based incentives
- Learning and development programs
- Exposure to global clinical trials
- Career growth opportunities in regulatory and clinical domains
Selection Process
The recruitment process generally includes:
- Application screening
- HR interview
- Technical/functional interview
- Final discussion and offer
How to Apply
Interested candidates can apply through the official online application process provided by Parexel. Ensure that your resume highlights relevant clinical research and regulatory experience before applying.
Important Dates
- Job Posted: Recently (Apply as soon as possible)
Why Apply for This Job?
Choosing the Site Start Up EUCTR I Job at Parexel can significantly enhance your career in clinical research. Here’s why:
- Opportunity to work with a globally reputed CRO
- Exposure to European clinical trial regulations (EUCTR & IVDR)
- Hands-on experience in clinical trial start-up processes
- Strong career growth in regulatory affairs and clinical operations
- Collaborative and professional work environment
- Skill development in project management and regulatory compliance
This role is ideal for candidates aiming to build expertise in international clinical trials and regulatory submissions.
FAQs
1. What is the main role of Site Start Up EUCTR I at Parexel?
The role focuses on managing EU clinical trial submissions, regulatory documentation, and coordination with study teams.
2. What qualifications are required for this job?
A Bachelor’s degree in Life Sciences or a related field with 1–2 years of relevant experience is required.
3. Is prior experience in EUCTR mandatory?
Basic knowledge is preferred but not mandatory. Training may be provided during the role.
4. What is the salary for this position?
The salary is offered as per company norms and may vary based on experience and skills.
5. How can I apply for this job?
You can apply through the official online application portal of Parexel.
Conclusion
The Site Start Up EUCTR I Job at Parexel 2026 is an excellent opportunity for early-career professionals in clinical research. With global exposure, structured learning, and a strong regulatory focus, this role can help you build a successful career in the pharmaceutical and clinical research industry. Interested candidates should apply at the earliest to secure this opportunity.
Disclaimer
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