Life Science Jobs at ClinChoice | BS Graduates Apply for the Associate Role
ClinChoice is seeking a motivated Regulatory Affairs Associate (Medical Devices) to join our hybrid team in Raritan, NJ. This role offers an exciting opportunity to contribute to impactful regulatory projects, support cross-functional teams, and ensure compliance in the fast-evolving medical device sector. If you are passionate about regulatory affairs, detail-oriented, and eager to grow your career in a collaborative global CRO, weโd love to hear from you.
- Job Title: Associate, Regulatory Affairs – Medical Devices
- Location: Raritan, New Jersey, United States
About the Company
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 28 years of proven high-quality delivery and results across all services, and a team of over 4,000 professionals in more than 20 countries, we are dedicated to contributing to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.
Responsibilities
- Assist in planning and tracking long-term regulatory projects and submission timelines.
- Regularly communicate with clients to understand their needs and address them proactively.
- Coordinate cross-functional team meetings to ensure project milestones are met.
- Maintain accurate project documentation and drive regulatory updates.
- Contribute to the development and improvement of regulatory project management processes.
- Track project deliverables and identify and escalate issues in a timely manner.
- Provide independent advice on project management based on experience.
- Assist in the preparation of RFI/RFPs/defense bid.
Skills
- Bachelorโs degree in Life Sciences, Regulatory Affairs, Project Management or related field. 2+ years of experience in regulatory affairs or related role.
- Technical system skills, including MS Office, Power BI, etc.
- Strong organizational and time management skills.
- Excellent written and verbal communication skills.
- Ability to present complex information to various levels.
- Proficiency with Microsoft Office; experience with project management tools is a plus.
The Application Process
Upon submitting your CV, you will receive an acknowledgment if you meet the requirements for a phone interview as the first step. Unfortunately, due to the high volume of applications, we may not be able to respond individually to all applicants.
Keywords: Life Science Jobs at ClinChoice, Job Posting, Regulatory Affairs, Medical Devices, Raritan, New Jersey, CRO, Professional Development, Work-Life Balance, Project Management, Healthcare, Life Sciences
