Clinical Affairs Professional

We’re looking for people who are determined to make life better for people around the world. Purpose Organization Background Our Medical Affairs Quality Content Review Group is dedicated to ensuring the highest standards of medical quality, accuracy, and compliance across all our endeavors, ensuring our customers receive accurate and timely...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

**Position Summary**: **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...

**Position Summary**: **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...

Preferred Education: Masters degree in a life science or biomedical engineering discipline preferred, or equivalent regulatory/writing experiencePreferred Experience: 1. The expected experience is 46 years with minimum 12 years of PSUR writing and reviewing experience. Significant experience writing scientific, medical/clinical, and technical content. 2....

1. Assisting Regulatory Stack preparation. 2. Assisting Medical affair contents management and creation. 3. Assisting teams across departments, in their regulatory compliance adherence. 4. Ability to research articles to relate regulatory and clinical needs to relevant technology(s). **Job Types**: Fresher, Internship Contract length: 6...

Regulatory Professional I - Clinical trial Submission **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN**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...

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...

We're expanding and have exciting new global clinical trial projects across the globe that need your expertise to grow.Who are we?A premier clinical research organization founded in Asia-Pacific with over 20 years of experience and a team of ~500 professionals managing operations in 39+ locations.We offer a full range of clinical trial services to various...

**Position Summary**: 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...

Job Title : Clinical Research Associate (CRA) Company : MS Clinical Research Pvt Ltd About 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...

. Department: Regulatory Affairs Rare Blood Disorders Job Level: 6 Are you passionate about driving regulatory strategy and life cycle management of product portfolio ensuring interactions with regulatory authorities across the globe? Do you thrive in a multi-disciplinary environment requiring a unique combination of scientific insights and...

. Department: Regulatory Affairs Rare Blood Disorders Job Level: 6 Are you passionate about driving regulatory strategy and life cycle management of product portfolio ensuring interactions with regulatory authorities across the globe? Do you thrive in a multi-disciplinary environment requiring a unique combination of scientific insights and...

Company Description:MS Clinical Research is a dynamic and innovative organization dedicated to advancing healthcare through clinical research. We are committed to excellence in every project, ensuring that our clients receive the most accurate and competitive quotes for their clinical studies.Job Summary:We are seeking a detail-oriented and analytical...

**Job Description: Clinical Research Trainee** **Position Overview**: A Clinical Research Trainee is an entry-level role within the field of clinical research, responsible for assisting in the planning, coordination, and execution of clinical trials and research studies aimed at evaluating the safety, efficacy, and effectiveness of new medical treatments,...

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...

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: 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 : Clinical Research Associate (CRA) Company : MS Clinical Research Pvt Ltd About 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...

Job Title: Clinical Research CoordinatorCompany: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a dynamic and forward-thinking clinical research organization dedicated to conducting cutting-edge clinical trials. We are committed to advancing medical science and contributing to the development of innovative healthcare solutions.Job...