Employer Industry: Clinical Research Services

Why Consider this Job Opportunity:
- Competitive salary
- Opportunities for career advancement and growth within the organization
- Flexible working culture with a focus on work-life balance
- Supportive and collaborative team environment
- Extensive benefits package focused on employee health and well-being

What to Expect (Job Responsibilities):
- Prepare, review, and coordinate local regulatory submissions in alignment with global submission strategy
- Provide regulatory strategy advice to internal clients
- Coordinate with internal departments to ensure site start-up activities align with submission activities
- Maintain trial status information and study files accurately
- Understand and adhere to PPD SOPs, Client SOPs, and current regulatory guidelines

What is Required (Qualifications):
- Bachelor's degree or equivalent
- 2+ years of relevant experience
- Effective communication skills
- Strong attention to detail and quality of documentation
- Basic knowledge of regional/national country regulatory guidelines and EC regulations

How to Stand Out (Preferred Qualifications):
- Basic medical/therapeutic area and medical terminology knowledge

#ClinicalResearchServices #CareerGrowth #WorkLifeBalance #CompetitiveSalary #TeamEnvironment

We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.