Pre-Development & Site Assessment Studies Coordinate site identification, screening, selection, feasibility assessment, and project development studies for proposed nuclear power projects. Manage consultants and technical agencies Monitor study schedules, deliverables, budgets, and interfaces across multiple agencies. Support preparation of
About Business: Adani Group: Adani Group is a diversified organisation in India comprising 10 publicly traded companies. It has created a world class logistics and utility infrastructure portfolio that has a pan-India presence. Adani Group is
Career CategoryInformation Systems Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all
Career CategoryResearch Job Description Role Name: Study Delivery Senior Associate Role GCF: 4 ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer.
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cepheid, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all
Career CategoryRegulatory Job Description ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines
Summary of Responsibilities: Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs), confidentiality agreements, amendments, and related site contract documentation. Coordinate with sponsors, legal teams, clinical operations, and study teams to facilitate timely contract execution. Manage site
Company: Novo Nordisk Global Business Services (GBS) Shape regulatory strategies that bring life-changing medicines from development through approval – and into the hands of patients across the globe. Your new role As a CMC Regulatory Specialist, you will
Role Description Responsibilities: This role reports directly into the Regional RA Lead for Africa, Southeast Asia, and South Asia. It spans across India and the Distributer Markets of Bangladesh, Nepal and Sri Lanka (BNS). The incumbent
Regulatory Consultant (CMC-EU, GCC & AU) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them
Career CategoryClinical Development Job Description This position requires People Management experience, Resource Allocation/Planning/Management experience ABOUT THE ROLE Role Description: The Manager, CSS is accountable for hiring, managing, mentoring and growing a team of Study Delivery Associates and
Job Purpose: Position Summary The Manager, Regulatory Compliance APJ is responsible for leading and supporting export compliance activities across the Asia Pacific region with India being a key focus market. This role will be based in India
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Safety & PV Specialist II - (4 + Years of experience in Clinical Studies) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across
Career CategoryRegulatory Job Description Job Description: Amgen is a leading human therapeutics company in the biotechnology industry. For more than 40 years, the company has tapped the power of scientific discovery and innovation to advance the
The Regulatory Affairs Senior Associate will work at the interface of R&D and Regulatory, building a genuine technical understanding of the products formulation and analytical profile to support sound regulatory strategy. This is not a document-processing role — it
The Regulatory Affairs Manager (Pre- Approval) will lead regulatory strategy and submission readiness for assigned development products from early development through first approval. The role integrates product, formulation, process, analytical, stability, nonclinical, clinical and device information, as applicable,
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and
Our Team: Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital
About SKF SKF started its operations in India in 1923. Today, SKF provides industry leading automotive and industrial engineered solutions through its five technology-centric platforms: bearings and units, seals, mechatronics, lubrication solutions and services. Over the