Project Manager Regulatory Affairs Vacancy – ClinChoice


Clinchoice
Project Manager Regulatory Affairs Vacancy – ClinChoice, India
Apply for Project Manager, Regulatory Affairs at ClinChoice, India. Open for Life Sciences graduates with 2-5 yrs experience.
Step into a career where your regulatory expertise can make a real impact. ClinChoice, a global full-service Contract Research Organization (CRO), is seeking a talented and motivated Project Manager in Regulatory Affairs to join its India team. This role offers an exciting opportunity to lead high-impact regulatory projects while contributing to innovative healthcare solutions on a global scale.
Company Overview
ClinChoice is a global leader in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 28 years of proven experience and 4,000+ professionals across 20+ countries, ClinChoice is committed to accelerating the development and commercialization of innovative drugs and devices.
ClinChoice’s “one-team” culture emphasizes quality, collaboration, and professional development. Employees are nurtured through continuous training and career growth opportunities, making ClinChoice not just a workplace but a platform to contribute meaningfully to global healthcare.
Job Role & Responsibilities
As a Project Manager, Regulatory Affairs, you will be the primary lead for assigned client projects, overseeing them from initiation through completion. Your core responsibilities will include:
- Leading regulatory projects, ensuring alignment with client and regulatory requirements.
- Developing and managing project plans, timelines, and deliverables.
- Coordinating internal teams, third parties, and vendors for seamless project execution.
- Monitoring project progress, identifying risks, and implementing mitigation strategies.
- Providing expert guidance and independent advice on project management.
- Contributing to RFI/RFP preparation and guiding the sales and business development team.
- Proactively identifying project risks and opportunities, escalating where appropriate.
This role is ideal for professionals who thrive in a fast-paced, multi-project environment and are passionate about driving successful regulatory outcomes.
Eligibility / Qualifications
Educational Requirements:
- Bachelor’s degree in Life Sciences, Regulatory Affairs, or related fields.
- Master’s or advanced degrees preferred; combination of Life Sciences and Business training is advantageous.
Experience & Skills:
- 2–5 years of experience in project management, preferably in a CRO or pharmaceutical setting.
- Strong organizational, interpersonal, and communication skills.
- Proven ability to manage multiple complex projects within strict deadlines.
- Proficiency in MS Office and project management tools.
- Excellent command of English (reading, writing, speaking).
Relevant Courses (LSI Keywords for SEO):
B.Sc in Life Sciences, B.Pharm, M.Pharm, Regulatory Affairs Certification, Clinical Research Training, MBA in Healthcare/Pharma Management
Location & Salary
Location: India (hybrid work model possible)
Salary: Competitive and commensurate with experience
Application Process
To apply, submit your CV/resume and cover letter via the official ClinChoice application portal. Steps include:
- Submission acknowledgement upon receiving your application.
- Screening based on eligibility and experience.
- Phone interview as the first step in the selection process.
⚠️ Due to high application volumes, only shortlisted candidates will be contacted.
Why Join ClinChoice?
- Global Impact: Contribute to life-saving drugs and medical devices worldwide.
- Professional Growth: Continuous training, mentorship, and career development opportunities.
- Inclusive Culture: Diversity and inclusion are integral to ClinChoice’s ethos.
- Work-Life Balance: Supportive work environment with flexible policies.
FAQ
Q1: What is the minimum eligibility for this role?
A: Bachelor’s in Life Sciences or Regulatory Affairs, with 2–5 years of project management experience.
Q2: Is this role open for freshers?
A: No, candidates should have 2–5 years of relevant experience.
Q3: What is the hiring process like?
A: Submit your CV → Phone interview → Selection. Only shortlisted candidates are contacted.
Q4: Can I work remotely?
A: ClinChoice offers a hybrid work model; occasional office presence may be required.
Q5: Does ClinChoice provide training?
A: Yes, continuous professional training is part of the company’s growth culture.
Vertical Summary Table
Category | Details |
---|---|
Company | ClinChoice |
Vacancies | 1+ (Project Manager, Regulatory Affairs) |
Required Education | B.Sc Life Sciences, B.Pharm, M.Pharm, Regulatory Affairs Certification, MBA in Healthcare/Pharma Management |
Experience | 2–5 years in Project Management, preferably in CRO/Pharma |
To apply for this job please visit job-boards.eu.greenhouse.io.