Remote Regulatory Affairs Job at Parexel, UK
Looking for a career in regulatory affairs with biologics or vaccines? This Remote Regulatory Affairs Job at Parexel Careers in the UK offers a chance to work in a dynamic, global environment while helping bring life-saving products to market. Join a collaborative team as a Regulatory Affairs Associate and build expertise in regulatory submissions and project management.
About the Company:
Parexel is a leading consulting and clinical research organization that supports biopharmaceutical and medical device companies. The company helps clients navigate complex regulatory landscapes and accelerate product approvals. Parexel focuses on innovation, collaboration, and continuous learning, offering employees global exposure and professional growth opportunities.
Job Details:
- Job Title: Regulatory Affairs Associate – CMC Biologics or Vaccines
- Location: United Kingdom (Remote)
- Additional Locations: Croatia, Poland, Romania, Serbia (Remote/Hybrid options)
- Job ID: R0000040278
- Category: Regulatory Affairs
- Work Mode: Remote / Home or Office Based
Role Responsibilities:
- Manage lifecycle maintenance activities, including renewals, variations, and responses to deficiency letters, in this Remote Regulatory Affairs Job in the UK
- Coordinate submission and management work in Veeva Vault
- Collaborate with various stakeholders, attending regular calls and meetings
- May serve as Project Lead for small-scale projects or Work Stream Lead on larger projects as a Regulatory Affairs Associate
- Ensure the project team delivers high-quality work meeting client expectations and timelines
- Manage project financials and identify new business opportunities
- Deliver consulting services within your area of expertise in this Regulatory Affairs Job at Parexel Careers
- Maintain professional interactions with clients and internal teams
Skills and experience required for the role:
- University degree in a life science discipline
- Initial years of regulatory experience in the UK, EU, and other non-EU markets preferred
- Proficiency in Module 1 and 3 writing with biologics and/or vaccines
- Strong organizational and prioritization skills
- Excellent communication and teamwork abilities
- Ability to work independently and under the guidance of Project Leads or Technical SMEs
- Commitment to continuous learning and self-development
- Fluent in English, written and spoken.
Benefits of the Regulatory Affairs Job:
- Remote work flexibility across multiple European locations
- Exposure to diverse clients and therapeutic areas
- Opportunities for career growth and skill development
- Mentorship from experienced regulatory professionals
- Collaborative and innovative work environment
- Involvement in impactful healthcare and life science projects
