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Showing posts with the label Clinical Data Management

"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs"

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"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs" (Syneos Health Hiring Safety & PV Coordinator in Hyderabad) Introduction Candidates looking to build a strong and long-term career in Pharmacovigilance (PV) and Drug Safety have an excellent opportunity at Syneos Health , a globally recognized biopharmaceutical solutions organization. Syneos Health is currently hiring for the position of Safety & PV Coordinator at its Hyderabad office . This is a full-time, office-based role , ideal for professionals who have experience or exposure in pharmacovigilance submissions, safety reporting, regulatory compliance, and clinical research processes . Working with a global organization like Syneos Health provides exposure to international safety regulations, cross-functional teams, and structured career growth . About The Company – Syneos Health Syneos Health® is a fully integrated biopharmaceutical solutions organization that supports pha...

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"Senior Clinical Data Associate Job in Ahmedabad – Advanced Clinical Hiring | Apply Now"

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"Advanced Clinical Hiring Senior Clinical Data Associate in Ahmedabad – 2025-26 Fast  Apply Now " (Senior Clinical Data Associate Job in Ahmedabad) If you’re aiming to build a strong and rewarding career in Clinical Data Management , this new opening from Advanced Clinical could be the perfect opportunity for you. Advanced Clinical is a well-known global clinical development organisation committed to providing high-quality, patient-centred research solutions. With a strong reputation in the global pharma and biotech industry, the company is expanding its India operations and is now hiring an experienced Senior Clinical Data Associate in Ahmedabad. About Advanced Clinical:- Advanced Clinical is an international Clinical Research Organisation (CRO) offering full-service clinical development, biometrics, and strategic resourcing services. The company works with global pharmaceutical, biotech, and medical device organisations to deliver safe and effective clinical trials. ...

“IQVIA Hiring Clinical Data Management Lead in Pune | Pharma Jobs 2025”

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"IQVIA Hiring Clinical Data Management Lead in Pune | Apply Now." (IQVIA Clinical Jobs 2025) (IQVIA Hiring Clinical Data Management Lead in Pune) Are you looking to advance your career in Clinical Data Management (CDM) with a globally recognized healthcare organization? IQVIA , a world leader in clinical research, healthcare intelligence, and advanced analytics , is hiring a Clinical Data Management Lead for its Pune location. This role is perfect for experienced CDM professionals who want to lead global clinical trials, ensure regulatory compliance, and drive data excellence across high-impact projects. About IQVIA:- IQVIA is a global powerhouse in clinical research and healthcare analytics, operating in more than 100 countries . The company supports pharmaceutical, biotech, and medical device organizations by delivering end-to-end clinical development and real-world evidence solutions . With a strong focus on innovation, digital transformation, and patient safety,...

"Process Solutions Marketing Operations Careers | Analyst Jobs in Bangalore 2025"

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"Analyst – Process Solutions Marketing Operations Jobs in Bangalore | Apply Now" (Process Solutions Marketing Operations) Are you a Life Sciences postgraduate looking to grow your career in product life cycle management and marketing operations ? A leading global healthcare, life sciences, and electronics company is inviting applications for the role of Analyst – Process Solutions Marketing Operations in Bangalore, Karnataka . This opportunity is perfect for candidates with 1–2 years of industry experience who want to contribute to product portfolio management, cross-functional collaboration, and process improvement in a globally recognized organization. Key Responsibilities:- As an Analyst – Process Solutions Marketing Operations, you will: Support Product Managers, Marketing Managers, and Project Managers with product life cycle management tasks. Collaborate with cross-functional teams including Manufacturing, Purchasing, QA, and Technical Services. Manage pr...

"Medical Writing Jobs 2025 | Samahitha Hiring Life Science Graduates (Immediate Joiners)"

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"Samahitha Hiring Life Science Graduates for Junior Medical Writer Role – Apply Now" (Medical Writing Jobs 2025) Samahitha, a reputed organization in the clinical research and healthcare industry , is inviting applications for the position of Junior Medical Writer . This is an excellent opportunity for Life Science graduates with 1–2 years of medical writing experience who are looking to advance their careers in a dynamic and growth-oriented environment. The role involves working on regulatory documents, clinical trial protocols, and scientific writing that contribute to international healthcare and pharmaceutical projects. Immediate joiners are preferred. Job Responsibilities:- As a Junior Medical Writer at Samahitha , your key responsibilities will include: Drafting and reviewing clinical trial protocols, investigator brochures, informed consent forms, and regulatory submissions . Preparing safety narratives, clinical study reports, and scientific manuscripts . E...

"Pharma Careers at Novamed Laboratories – Apply Now for QC, QA, Production, and Engineering Roles"

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"Novamed Laboratories Hiring for Multiple Pharma Roles in Bahadurgarh (Delhi NCR) – Apply Now" Are you ready to build a rewarding career in the pharmaceutical industry? Novamed Laboratories , a leading name in topical patch manufacturing , is conducting recruitment for multiple positions at its USFDA-compliant facility in Sector 16, Bahadurgarh, Haryana (Delhi NCR) . With the largest production capacity in the region and cutting-edge technology, Novamed offers exciting career opportunities in Production, Quality Assurance (QA), Quality Control (QC), Engineering, IT, Procurement, and EHS . If you are passionate about pharma manufacturing and regulatory excellence, this is your chance to join a fast-growing global healthcare company . Available Positions:- 1. Assistant Manager – Production Lead production operations for transdermal patches . Ensure compliance with USFDA and global standards . Guide and manage production teams to achieve targets. 2. Officer – Product...

"Clinical Research Monitor Jobs at St Johns Medical College Bangalore | Apply for TIPS-3 PHRI Study"

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"Clinical Research Monitor Jobs at St John's Medical College, Bangalore | Apply Now for TIPS-3 PHRI Study." (Clinical Research Monitor Jobs at St John's Medical College, Bangalore) St John's Medical College, one of the most prestigious medical institutions in Bangalore, is inviting applications for the position of Clinical Research Monitor for the TIPS-3 PHRI Study . This is an excellent opportunity for healthcare and life sciences professionals to build a rewarding career in clinical research while contributing to global medical advancements. Job Responsibilities:- As a Clinical Research Monitor , you will be responsible for ensuring the smooth and ethical conduct of the TIPS-3 PHRI clinical trial. Your primary duties will include: Clinical Trial Monitoring : Oversee trial sites to ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. Data Verification & Reporting : Review and validate clinical data, preparin...

"Career Opportunity: Executive – Regulatory Affairs in Healthcare Industry"

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"Executive – Regulatory Affairs Job in Bengaluru | Global Healthcare Company Hiring" (Career Opportunity: Executive) Introduction Pharmaceutical and medical device regulatory professionals are currently witnessing strong demand across India, especially in metro cities like Bengaluru. With the rapid growth of medical device regulations under India MDR, global healthcare companies are actively hiring skilled regulatory experts. A leading global healthcare and technology-driven organisation has announced an excellent career opportunity for the position of Executive – Regulatory Affairs in Bengaluru, India . This role is ideal for professionals who already have hands-on exposure to India Medical Device Rules (MDR) and want to build a long-term career in regulatory compliance, licensing, and international coordination. If you have 1–3 years of regulatory affairs experience , this position can be a strong stepping stone toward global regulatory roles. About the Company The hirin...

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