Medical Regulatory Executive

Hi Opening with a client into medical Devices at Nayandahalli Job Description Job Title: Sr. Executive - Regulatory Affairs Reporting To: RA Manager. Key responsibilities Duties: - Experience in preparation of Device master file and other documents as per CDSCO MDR-17 requirements and submission of documents in CDSCO portal. - Experience in preparation...

ClinChoice Medical Writing RoleJob SummaryClinChoice is seeking a highly skilled Regulatory Medical Writer to support our clinical research initiatives. The ideal candidate will have strong clinical/scientific writing skills and experience in medical writing for regulatory submissions.ResponsibilitiesResearch, create, edit, and coordinate the production of...

Job Title: Medical, Legal and Regulatory Reviewer (MLR)The Medical, Legal and Regulatory (MLR) review process is a critical component of healthcare marketing, ensuring that advertising, promotional, and non-promotional content is accurate, compliant, and ready for publication. As an MLR Reviewer, you will play a key role in rigorously controlling and...

Regulatory Professional **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN**Department: Research & Development** - Do you want to play a key role in accelerating the development of our patient-focused products? Are you passionate about regulatory science and executing on regulatory strategies to bring innovative...

Job Description: Medical Content WriterLocation: Jayanagar 3rd Block, Bangalore, IndiaExperience: 3 to 6 YearsBudget: 4 to 6 Lakh INR per annum About Us: We are a leading healthcare organization dedicated to providing high-quality medical content to healthcare professionals and patients alike. Our mission is to make medical knowledge accessible and...

ClinChoice is seeking a highly skilled Regulatory Document Medical Writer to join our team.About the Role:The Medical Writer will be responsible for researching, creating, editing, and coordinating the production of clinical and regulatory submission documents, including clinical study reports, protocols, CTD sections, IB, and safety update...

**Company Description** In cooperation with affiliate / Area Medical teams, Marketing, RA, Clinical and other functional areas, provides leadership, oversight and support for assigned products/projects. Establishes and approves scientific methods for hypotheses, rational, design of affiliate/Area/Global protocols and their reports. Participation in design...

In cooperation with affiliate / Area Medical teams, Marketing, RA, Clinical and other functional areas, provides leadership, oversight and support for assigned products/projects. - Establishes and approves scientific methods for hypotheses, rational, design of affiliate/Area/Global protocols and their reports. - Participation in design and execution of...

Provide responses to regulatory agencies regarding product information or issues. - Train RA Assistant and staffs in regulatory policies or procedures. Coordinate internal discoveries and depositions with legal department staff. - Develop and maintain standard operating procedures or local working practices. - Establish regulatory priorities or budgets and...

Job SummaryClinChoice is seeking a skilled Senior Medical Writer to join our team. The ideal candidate will have experience in medical writing for regulatory documents, such as clinical study reports, protocols, and CTD sections.Key Responsibilities:Research and create high-quality clinical documents for regulatory submissions.Collaborate with project teams...

Clinical and Regulatory Submissions Medical WriterAt ClinChoice, we are seeking a highly skilled Medical Writer to join our team.About the RoleThe Medical Writer will research, create, edit, and coordinate the production of clinical and regulatory submission documents, including clinical study reports, protocols, CTD sections, IB, and safety update...

Clinical Document SpecialistClinChoice is seeking a highly skilled Clinical Document Specialist to join our team. As a Clinical Document Specialist, you will be responsible for researching, creating, editing, and coordinating the production of clinical and regulatory submission documents.Key Responsibilities:Research and create clinical and regulatory...

Job Title: Senior Medical Writer/Medical WriterVCLS is a leading provider of medical writing services in the pharmaceutical industry. We are seeking a highly skilled Senior Medical Writer/Medical Writer to join our team.Key Responsibilities:Author high-quality medical documents for client projects, including study protocols, investigator brochures, and...

Key Role in Clinical Research Document CreationAt Parexel, we are seeking a skilled Regulatory Medical Content Specialist to join our Medical Writing Services team. In this critical role, you will research, create, and edit documents associated with clinical research.Key Responsibilities:Research and create high-quality clinical research documents, including...

Parexel is seeking a highly skilled Regulatory Medical Writing Lead to join our team.The successful candidate will have experience in creating and editing documents associated with clinical research, including protocols, clinical study reports, and investigator's brochures.Key responsibilities include:Researching and authoring high-quality...

Regulatory Professional **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Bangalore, Karnataka, IN**Department**:RA CMC & Device**About the Department** - RA CMC & Device Bangalore in Global Business Services (GBS) Bangalore is a part of Bangalore Global Development hub consisting of high calibre regulatory professionals. The objective of the...

**The Position**: Will be responsible for executing medical affairs strategy in the assigned zone. **Tasks & Responsibilities**: - Understand the current practices, medicines being used, and trends in relation to their respective therapeutic area through key customer contacts, attending scientific symposia and reviewing key therapeutic journals in order to...

Parexel: A Leading Provider of Medical Writing ServicesSenior Medical Writer RoleThe Senior Medical Writer will be responsible for creating and editing all documents associated with clinical research. As part of the Medical Writing Services team, this individual will operate as the project lead writer/submission coordinator and primary client contact to...

As a Medical Reviewer in Pharmacovigilance, you will play a crucial role in evaluating and assessing the safety of pharmaceutical products. Your primary responsibilities will include reviewing and analyzing adverse event reports, medical literature, and other safety-related information to ensure compliance with regulatory requirements and to contribute to...

**Department** - Tele sales Executive (Patient Care Executive) **Location** - Bangalore **Experience** - 1- 3 Years **Qualification**-B.Sc., B.Pharma **Location**: Bangalore **About the Role**: We are seeking a highly motivated and empathetic Patient Care Executive to join our growing Medical Equipment department. This unique role combines your dedication...