jobson.way25@gmail.com Syneos Health is seeking a highly skilled Associate RA to join their team in a remote capacity. This role involves assisting with the preparation of Module 1 documents and regulatory submission documents, including components of Investigational New Drug Applications (INDs) and New Drug Applications (NDAs). 💼About the Role As an Associate RA, you will play … Read more
Samahitha is seeking a skilled Quality Control (QC) professional to join their team in Bengaluru, Karnataka. This role involves preparing audit plans, conducting audits, and reviewing reports to ensure compliance with regulatory requirements. 🔍About the Role As a Quality Control professional, you will play a critical role in ensuring the quality and integrity of clinical … Read more
Imaging Endpoints, a leading Imaging Technology and Imaging Clinical Research Organisation (iCRO), is seeking a skilled Clinical Project Coordinator to join their team. This role involves coordinating clinical project activities, managing trial master files, and ensuring compliance with regulatory requirements. 🔍About the Role As a Clinical Project Coordinator, you will play a critical role in … Read more
Macleods Pharmaceutical Ltd. is seeking a qualified and experienced Aggregate Report Reviewer to join their team in the Pharma Covigilance department at their R&D facility in Andheri, Mumbai. This role involves quality reviewing PSUR, PBRER, and ACO reports, as well as preparing and tracking reports for submission to regulatory authorities. About the Role As an … Read more
Location: HyderabadDepartment: R&D – Monoclonal Antibodies (Upstream – Media Optimisation) Virchow Biotech Pvt. Ltd. is seeking experienced professionals to join our R&D mAbs team as Sr. Executive / Assistant Manager (Upstream – Media Optimisation). This is an excellent opportunity to work with a leading biotech company known for innovation and excellence in biologics. About the … Read more
Vizen Lifesciences is seeking highly skilled Drug Safety Associates to join their team. If you’re a professional with 1-4 years of experience in Post-Marketing Surveillance (PMS) and hands-on experience with ARGUS Safety Database, this could be the perfect opportunity for you. 💊 About the Role As a Drug Safety Associate, you will be responsible for … Read more
Novotech, a leading clinical research organisation, is seeking a skilled Document Management Associate (DMA) to join its team. This role involves managing Trial Master Files (TMF) for clinical trials, ensuring compliance with regulatory requirements and company SOPs. 🧾About the Role As a Document Management Associate, you will play a critical role in supporting clinical teams … Read more
Cliantha is seeking a skilled QC Reviewer with clinic experience to join their team in Vadodara. This role involves reviewing clinical raw data for completeness, accuracy, and compliance with regulatory guidelines. 🧪About the Role As a QC Reviewer, you will play a critical role in ensuring the quality of clinical data. Your primary responsibilities will … Read more
Sun Pharma, a leading pharmaceutical company, is seeking a dynamic Regulatory Affairs professional to join its team in Vadodara. This role will focus on supporting ROW (Rest of the World) markets, specifically South Africa, Nepal, and MENA (Middle East and North Africa) regions. 🧩About the Role As a Regulatory Affairs Executive, you will play a … Read more
Are you a dynamic and results-driven individual with a passion for recruitment? Xpheno is hiring a Recruitment Coordinator in Hyderabad to join their talented team. As a Recruitment Coordinator, you will play a critical role in managing the recruitment process, ensuring that the best talent is identified and hired. 💼About the Role: Recruitment Management: Manage … Read more