Clinical Trial Protocol Specialist

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...

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

The position As Regulatory Professional, you will play a crucial role in driving, coordinating, and actively following up on multiple tasks with challenging timelines. Your responsibilities will include: Working closely with various submission teams across the organization and all countries in Europe Managing initial clinical trial application...

Department: EU Submissions Hub Are you ready to make a difference in the lives of millions of people living with a serious chronic disease? Join Novo Nordisk, a proud life-science company on a mission to ensure that people living with a chronic disease can live a full life. We are looking for a dedicated EU Submission Lead for Clinical Trials to...

Clinical Research Coordinator About the job Role Description This is a full-time hybrid role for a Clinical Research Coordinator with Client. The Clinical Research Coordinator will be responsible for day-to-day tasks related to clinical research, including informed consent, protocols, research, clinical research experience, and clinical trials. This...

Clinical ResearchCoordinator Aboutthejob RoleDescription Thisis a fulltime hybrid role for a Clinical Research Coordinator withClient. The Clinical Research Coordinator will be responsible fordaytoday tasks related to clinical research including informedconsent protocols research clinical research experience andclinical trials. This role is located in...

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years of...

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow. Who are we? A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of...

Department – Data Management & Centralized Data Review Are you an experienced Project Clinical Data Programming Specialist with a strong background in the pharmaceutical industry? Do you have expertise in CDISC SDTM and a passion for driving quality set-up deliverables across the value chain? If so, we have an exciting opportunity for you to join...

Company Overview:iProcess is a leader in biospecimen collection studies, providing key contributions to the advancement of medical research. Our speciality in the procurement and handling of quality biospecimens underpins crucial developments in medical diagnostics and therapies. For more information about our dedicated approach to medical research, visit ...

Company Overview: iProcess is a leader in biospecimen collection studies, providing key contributions to the advancement of medical research. Our speciality in the procurement and handling of quality biospecimens underpins crucial developments in medical diagnostics and therapies. For more information about our dedicated approach to medical research, visit ...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

About the job TMF Specialist is to perform all duties related to the timely processing of essential and non-essential clinical trial documents to facilitate study startup, drug shipment, eTMF maintenance and support eTMF inspection readiness activities Location : Bangalore/Chennai Experience Skills Ability to interact with Clinical and Regulatory team...

Company Overview:iProcess is a leader in biospecimen collection studies, providing key contributions to the advancement of medical research. Our speciality in the procurement and handling of quality biospecimens underpins crucial developments in medical diagnostics and therapies. For more information about our dedicated approach to medical research, visit...

Job Description :You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical,...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Position Title : Executive / Assistant Manager - Clinical Operations (Clinical Research Associate)Location : BangaloreAt VIATRIS™, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.Viatris empowers people worldwide to live healthier at...

Company DescriptionMS CLINICAL RESEARCH PRIVATE LIMITED was established in 2009. MSCR is a team of experienced medical specialists, life science graduates, and management and process experts with a keen research interest. MSCR aims to be the globally preferred comprehensive dermatology research testing organization specialized in skin of color. Maintaining...