Regulatory Affairs Director

4 weeks ago


Bengaluru, Karnataka, India Parexel Full time

About this role

We are seeking a highly experienced Regulatory Affairs Director to join our team at Parexel. As a key member of our regulatory team, you will be responsible for ensuring the successful submission of clinical trial regulatory documents.

Key Responsibilities

  • Clinical Trial Regulatory Submissions: Over 15 years of relevant experience in clinical trial regulatory submissions.
  • Regulatory Leadership: Experience in managing clinical trial studies, serving as Regulatory Lead for global trials, with exposure to the European market.
  • Database Expertise: Proficiency in handling the CTIS database and submitting EU CTR and CDSCO is desirable.
  • Project Profitability: Monitor the profitability of multiple projects/programs through active involvement with project leads in preparing project plans and managing project budgets.
  • Revenue Recognition: Proactively avoid and resolve issues with revenue recognition.
  • Team Collaboration: Work within a team environment or individually based on project needs.
  • Mentorship: Provide guidance to project team members and act as a mentor to staff.
  • Issue Resolution: Work within broad project guidelines and lead issue and conflict resolutions.
  • Workload Management: Prioritize own workload and the workload of the project team to achieve project scope and objectives.
  • Efficiency Improvement: Capitalize on opportunities to improve project efficiency, results, or team performance and proactively take action.
  • Performance Management: Actively manage performance, including typical HR activities for direct reports (e.g., performance management reviews, salary actions, bonuses, scorecards).
  • Staff Support: Provide input on staff to appropriate PC Members and support direct reports with the management of their staff.
  • Guidance and Accountability: Provide applicable guidance and support to staff to succeed and achieve key metrics; hold staff accountable to key metrics.
  • Staff Development: Facilitate staff development plans and coordinate with Strategic Resourcing staffing to ensure staff is utilized completely and appropriately to increase their expertise.
  • Skill Expansion: Collaborate with strategic resourcing to provide staff with opportunities to expand skill sets.
  • Recognition and Reward: Reward staff appropriately as needed.
  • Leadership and Mentoring: Provide leadership, coaching, mentoring, feedback, and role modeling to managers and extended staff to ensure quality and accuracy of services as well as achievement of key metrics.
  • Vision and Values Communication: Communicate and champion organizational vision and values.
  • Effective Communication: Regularly communicate with staff to assure effective two-way information flow (e.g., business updates, staff interests, issues, and/or concerns).
  • Consulting Services: Provide a full range of technical and/or business consulting services mainly in areas where policy or precedent is clear.
  • Self-Development: Define self-development activities to keep current within the industry (e.g., maintain membership in a relevant industry and/or scientific/technical association).
  • Project Efficiency: Capitalize on opportunities to improve project efficiency, results, or team performance and proactively take action.
  • Information Leverage: Leverage information from previous projects or other client work to efficiently complete assigned project activities and facilitate business decisions.
  • Quality Work: Produce quality work that meets the expectations of the client. Review the work of colleagues for content and quality to ensure client and PC expectations are met.
  • Strategy Development: Assess project issues and develop strategies to meet productivity, quality, and project goals and objectives.
  • Performance Management: Actively manage performance, including typical HR activities for direct reports (e.g., performance management reviews, salary actions, bonuses, scorecards)


  • Bengaluru, Karnataka, India Parexel Full time

    Director of Regulatory Affairs and Clinical TrialsWe are seeking a highly experienced Director to lead our regulatory affairs and clinical trials team.About the RoleThis is a senior leadership position that will oversee the strategic direction of our regulatory affairs and clinical trials operations.Key ResponsibilitiesProvide strategic guidance on...


  • Bengaluru, Karnataka, India Parexel Full time

    Job TitleAssociate Director, Regulatory AffairsAbout the RoleParexel is seeking an experienced Associate Director, Regulatory Affairs to join our team. The ideal candidate will have a strong background in clinical trial regulatory submissions and leadership experience in managing clinical trial studies.Clinical Trial Regulatory Submissions: Over 15 years of...


  • Bengaluru, Karnataka, India Parexel Full time

    Unlock Your Potential in Regulatory AffairsAt Parexel, we're seeking a highly skilled Regulatory Affairs professional to join our team. As a Regulatory Affairs Director, you will play a critical role in ensuring the success of our clinical trials by providing expert guidance on regulatory submissions and compliance.10+ years of experience in Clinical Trial...


  • Bengaluru, Karnataka, India Lifelancer Full time

    **About Lifelancer**Lifelancer is a global talent-hiring platform that connects professionals with opportunities in the life sciences, pharma, and IT industries. Our goal is to help individuals advance their careers while promoting equal opportunities for people with disabilities. **Company Overview**Lilly is a global healthcare leader headquartered in...


  • Bengaluru, Karnataka, India Parexel Full time

    About the RoleParexel is seeking a skilled Senior Regulatory Affairs Director to lead clinical trial regulatory submissions and regulatory leadership initiatives. As a key member of our team, you will be responsible for managing clinical trial studies, serving as the regulatory lead for global trials, and providing guidance to project team members.Clinical...


  • Bengaluru, Karnataka, India Parexel Full time

    Empowering Excellence in Regulatory Affairs At Parexel, we are committed to delivering exceptional results and quality services. As an Associate Director of Regulatory Affairs, you will play a critical role in ensuring the success of our clinical trials and regulatory submissions. Key Responsibilities Clinical Trial Regulatory Submissions : Over 15...


  • Bengaluru, Karnataka, India Parexel Full time

    About the RoleWe are seeking a highly experienced Regulatory Affairs Director to join our team at Parexel. As a key member of our regulatory team, you will be responsible for leading clinical trial regulatory submissions and providing regulatory leadership for global trials.Key ResponsibilitiesClinical Trial Regulatory Submissions: Over 15 years of relevant...


  • Bengaluru, Karnataka, India Parexel Full time

    About the RoleParexel is seeking a highly experienced Regulatory Affairs Director to lead our clinical trial regulatory submissions team. As a key member of our team, you will be responsible for managing global trials, ensuring compliance with regulatory requirements, and providing guidance to project teams.Key ResponsibilitiesClinical Trial Regulatory...


  • Bengaluru, Karnataka, India Baxter Full time

    Regulatory Affairs at Baxter: A Key Role in Delivering Innovative Healthcare SolutionsBaxter, a leading medical products company, is seeking a talented Regulatory Affairs Specialist to join its team. In this crucial role, you will play a key part in ensuring the company's products meet the highest regulatory standards, enabling us to deliver innovative...


  • Bengaluru, Karnataka, India Philips Full time

    Job Title: Sr. Regulatory Affairs SpecialistYou will be an integral member of our Clinical Informatics Regulatory Affairs team, influencing and shaping the regulatory capabilities for future success of Philips.Your Key Responsibilities:Ensure safe and effective products/solutions are brought to market on time and sustained throughout their lifecycle via...


  • Bengaluru, Karnataka, India Biocon Biologics Full time

    Job Title: Manager Global Regulatory AffairsAt Biocon Biologics, we are seeking a highly skilled and experienced Manager Global Regulatory Affairs to join our team.Key Responsibilities:Develop and execute global regulatory strategies for biosimilar products, ensuring compliance with regulatory requirements and industry standards.Collaborate with...


  • Bengaluru, Karnataka, India Lifelancer Full time

    Company OverviewLifelancer is a leading talent-hiring platform in the Life Sciences, Pharma, and IT sectors. Our mission is to connect top talent with opportunities in these fields. Job Title: Regulatory Affairs ManagerSalary: $120,000 - $180,000 per yearLocation: Remote or On-Site (Flexible)Job Description:We are seeking an experienced Regulatory Affairs...


  • Bengaluru, Karnataka, India Indegene Full time

    Job Title: Regulatory Affairs LeadAt Indegene, we are seeking a highly skilled Regulatory Affairs Lead to join our team. This role will be responsible for ensuring compliance with regulatory requirements for medical devices worldwide.Key Responsibilities:Disseminate regulatory intelligence and coordinate with stakeholders to ensure compliance.Assess...


  • Bengaluru, Karnataka, India Parexel Full time

    About the RoleParexel is seeking a highly skilled Regulatory Affairs professional to join our team. As a Regulatory Affairs Consultant, you will be responsible for managing the pre- and post-approval life cycle of biologic products in various markets, including regulated (EU/US/Canada) and emerging markets.Key ResponsibilitiesDevelop and implement regulatory...


  • Bengaluru, Karnataka, India ResMed Full time

    The Regulatory Affairs function at ResMed plays a crucial role in ensuring compliance with regulatory frameworks and delivering optimal regulatory strategies for portfolio planning, active regulatory intelligence, and excellence in execution.Key Responsibilities:Support and maintain various internal and government databases relevant to ResMed's...


  • Bengaluru, Karnataka, India Baxter Full time

    About VantiveVantive is a new company built on the legacy of Baxter, a leading healthcare company. We are on a mission to revolutionize kidney care and other vital organ support.Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team. The successful candidate will be responsible for supporting all regulatory activities...


  • Bengaluru, Karnataka, India Indegene Full time

    Regulatory Affairs LeadThe ideal candidate for this role will be a highly organized and detail-oriented individual with a strong background in Medical Device Regulations. As a Regulatory Affairs Lead at Indegene, you will be responsible for ensuring compliance with global regulations and facilitating the registration of medical devices.Key...


  • Bengaluru, Karnataka, India Baxter Full time

    Transforming Healthcare, One Document at a TimeBaxter is a global leader in medical innovations, and we're looking for a skilled Regulatory Affairs Specialist to join our team.As a Regulatory Affairs Specialist at Baxter, you'll play a critical role in ensuring the accuracy and compliance of regulatory documentation for our medical products.Responsibilities...


  • Bengaluru, Karnataka, India Baxter Full time

    Regulatory Role at BaxterBaxter is a leading company in the healthcare industry, and we are seeking a highly skilled Regulatory Affairs Specialist to join our team. In this role, you will be responsible for providing regulatory support for on-market products, ensuring compliance with regulatory requirements, and identifying opportunities for process...


  • Bengaluru, Karnataka, India Philips Full time

    Job Title: Principal Regulatory Affairs SpecialistJob Description:The Principal Regulatory Affairs Specialist will play a key role in developing and executing the regulatory strategy for new product development, design changes, and field safety corrections for the US, EU, and RoW. This includes authoring 510k submissions, leading pre-sub meetings, creating...