Clinical Affairs

Job Description:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Allucent. As a key member of our Study Start-up & Site Intelligence department, you will play a vital role in ensuring the successful execution of clinical trials.About the Role:Coordinate and perform local site start-up activities, including document...

Reporting to: Assistant Manager – Regulatory Affairs Division: Ortho Implants Location: Chennai No. of Positions: 1 Education: B.E/ B. Tech in Biomedical Engineering / M. Pharm Regulatory Affairs Experience: 2 - 4 years Exp. in ‘scientific writing / clinical documentation’ role preferred KEY RESPONSIBILITIES: Technical writing, literature search,...

**Industry** Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position** Full Time, Permanent **Division** Pubrica Brand **Reports to**: Pubrica Business Head **About Company** Guires Group is a renowned global provider of services in advanced Contract Research, Data Science, Development, Pilot...

**Job highlights** - Years of Experience: Minimum 5 Years in Medical Device/ Pharma/ Life science. Qualification: M Sc Life Science/ BTech Medical / B Pharm/ M Pharm. - Minimum of 2-3 years of experience in regulatory affairs Healthcare industry, with specific experience in USFDA / 510K submission and MDSAP Audit preparation **Job description** This is a...

**Key Responsibilities**: - **Training Program Development**: - Develop and implement a robust training curriculum aligned with industry standards and regulatory requirements. - Create engaging training materials, including presentations, handouts, and online learning modules. - Design and deliver customized training programs to meet the specific needs of...

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds. ClinChoice, is searching for an Executive - Regulatory Affairs (PLMDS) to join one of our clients. **Main Job Tasks and Responsibilities**: - Complete...

We are seeking a skilled Regulatory Affairs Specialist to join our team at TTK Healthcare. In this role, you will be responsible for ensuring compliance with regulatory requirements for medical devices, specifically Class III products.Job Summary:Technical writing and data analysis as per guidelines for medical devicesScientific development of protocols and...

Job Summary The Regulatory Affairs Specialist is responsible for ensuring compliance with all applicable regulations governing the development, manufacturing, and distribution of the company's products. This role involves collaborating with internal teams and regulatory agencies to facilitate product registrations, approvals, and adherence to quality...

About LifelancerLifelancer is a pioneering talent-hiring platform in the Life Sciences, Pharma, and IT sectors. Our mission is to connect talented professionals with exciting opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains.Company OverviewSyneos Health is a leading fully integrated biopharmaceutical solutions...

**Key Responsibilities**: - **Regulatory Compliance**: Ensure compliance with ISO 13485, EU MDR 2017/745, US-FDA, CDSCO, and other applicable international standards for medical devices. - **Submissions and Approvals**: Prepare, review, and submit regulatory documentation, including 510(k) and IMDR submissions, to regulatory authorities such as US-FDA,...

About Syneos HealthWe are a leading fully integrated biopharmaceutical solutions organization, committed to accelerating customer success. Our Clinical Development model brings the customer and the patient to the center of everything we do.Our goal is to simplify and streamline our work, making Syneos Health easier to work with and easier to work for. We...

Company OverviewSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Estimated Salary: $60,000 - $80,000 per yearJob DescriptionA Medical Content Specialist will compile,...

**Industry** Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position** Full Time, Permanent **Division** Pubrica Brand **Reports to**: Pubrica Business Head **About Company** Guires Group is a renowned global provider of services in advanced Contract Research, Data Science, Development, Pilot...

We are looking for a **experienced/fresher dentist** in and around **chromepet **who's eager to learn. - working hours:_ - Morning shift 10am to 6.30pm - Evening shift 12.30pm to 9pm - Morning part time shift: 10am to 3.30pm - Evening part time shift: 4pm to 9pm. **Salary: Basic 15,000 + incentive starts at 3rd month**.(fresher), varies based on...

**Medical Writer Immediate Joiner** **Job description** **Industry**: Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position**: Intern **Reports to**: Pubrica Business Head **Work Schedule**: Full Time, Monday to Saturday, 10:00a.m. to 7:00pm. Hours may vary on occasion, depending on workload....

**Medical Writer Immediate Joiner** **Job description** **Industry**: Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position**: Intern **Reports to**: Pubrica Business Head **Work Schedule**: Full Time, Monday to Saturday, 10:00a.m. to 7:00pm. Hours may vary on occasion, depending on workload....

**Medical Writer Immediate Joiner** **Job description** **Industry**: Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position**: Intern **Reports to**: Pubrica Business Head **Work Schedule**: Full Time, Monday to Saturday, 10:00a.m. to 7:00pm. Hours may vary on occasion, depending on workload....

**Medical Writer Immediate Joiner** **Job description** **Industry**: Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position**: Intern **Reports to**: Pubrica Business Head **Work Schedule**: Full Time, Monday to Saturday, 10:00a.m. to 7:00pm. Hours may vary on occasion, depending on workload....

**Medical Writer Immediate Joiner** **Job description** **Industry**: Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position**: Intern **Reports to**: Pubrica Business Head **Work Schedule**: Full Time, Monday to Saturday, 10:00a.m. to 7:00pm. Hours may vary on occasion, depending on workload....

**Medical Writer Immediate Joiner** **Job description** **Industry**: Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position**: Intern **Reports to**: Pubrica Business Head **Work Schedule**: Full Time, Monday to Saturday, 10:00a.m. to 7:00pm. Hours may vary on occasion, depending on workload....