Regulatory and Clinical Business Analyst

Job Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical...

Job Title: Business Analyst – Life Sciences Domain Location: US / UK / India / Japan Experience Required: 5–8 years in Life Sciences / Pharmaceutical domain Job Summary Sonata Software is looking for a seasoned Business Analyst with 5–8 years of experience in the Healthcare and Life Sciences domain, with a strong focus on Clinical Trials and...

Business Analyst in Clinical TrialsWe are seeking a seasoned Business Analyst to join our team.The ideal candidate will have hands-on experience with clinical trial systems and have played a key role in 2–3 end-to-end technology implementations across the clinical trials value chain.This role demands a deep understanding of business processes, stakeholder...

Regulatory Manager Job DescriptionAs a Regulatory Manager, you will play a crucial role in ensuring compliance with regulatory requirements and facilitating the success of our clinical trials. Your expertise in regulatory submissions and experience in managing clinical trial studies will be invaluable to our team.Key Responsibilities:Manage clinical trial...

Regulatory reporting is a critical aspect of the financial industry, requiring meticulous attention to detail and a deep understanding of complex systems.About the RoleWe are seeking a Senior Business Analyst to join our team in this capacity. The ideal candidate will have experience in implementing and managing regulatory controls using third-party systems...

Job roleTo enable organisations emergence as a world class R&D organization, the Site Management and Monitoring (SMM) Country/District COM plays a leadership role accountable for driving the businessof SMM within a Country/District(s) by providing oversight and direction to SMM staff; accountable for the on time, within budget and quality delivery of the...

We are looking to add an experienced Clinical Writer to our team The person in this position must be able to independently contribute to the development of initial and update s of CER s that support the applicable regulatory submission requirements for the medical device products An experienced Clinical Analyst professional has relevant medical...

Senior CVA, Chennai, Office basedICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Senior Clinical Validation Analyst to...

Position Overview: The role of QTC Analyst, Senior is primarily responsible for direct action and oversight of the day-to-day operations of ensuring compliance for product release launch activities and post-launch compliance and ensuring compliance as set forth by regulatory agencies and endpoint Quality Management System (QMS) as well as participate and...

Global Regulatory Expert - Clinical and Medical WritingWe are seeking a highly skilled Global Regulatory Expert with expertise in clinical and medical writing. This role is responsible for handling complex projects and providing review support for deliverables that support the regulatory portfolio.This position requires strong knowledge of regulatory...