Medical Writing

Job Overview An entry level role within a structured program, supporting Medical Writing deliverables and focusing on specific tasks under senior supervision, while gaining experience, knowledge, and skills in Medical Writing. Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with...

Department – Clinical Reporting Unit Are you an experienced Medical Writing specialist with a strong background in regulatory medical writing? Do you have a passion for clear and concise communication of clinical data? We are looking for a Medical writing Specialist to join our Clinical Reporting team at Novo Nordisk. If you are ready for a new...

We’re looking for people who are determined to make life better for people around the world. Purpose:   Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across...

The position As a Medical Writing Specialist, you will be responsible for performing medical writing tasks of high complexity and acting as a project manager. Your role will involve planning, developing, and overseeing regulatory documents across all phases of clinical development. This includes but is not limited to, the preparation of Protocols,...

About ViatrisAt 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 every stage of life.We do so via:Access – Providing high quality trusted medicines regardless of geography or...

About ViatrisAt 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 every stage of life.We do so via:Access – Providing high quality trusted medicines regardless of geography or...

Design Hub Writing Roles - Regulatory & Medical Writing Global Captive Center of a Fortune 500 Pharmaceutical Organization Location - Bangalore (Relocation Mandatory) Experience - 2 to 10 years Mandatory Working Experience - Protocol Writing, Informed Consent Forms (ICFs) & Clinical Study Reports (CSRs) in Clinical Trials Phases 0 to IV. **Job Types**:...

Practices good internal and external customer service - Responsible for scientific medical writing and producing high quality documents - Understands ICH guidelines, as applicable to medical writing for clinical studies - Creates medical writing training exercises; mentors new medical writers - Trains via self-study and self-practice independently and...

Veranex is the only truly comprehensive, global, tech-enabled service provider dedicated to the medical technology industry. Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables...

oLead one or more assets and serve as a medical writing point of contact for this/these assets. Support prioritising workload across an asset (s)to deliver MW portfolio. oLead matrix team to drive the delivery of high quality, fit-for-purpose clinical documents that accurately reflect associated data and are in line with GSK standards and...

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...

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...

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...

Job Overview Acts as Lead Medical Writer on more advanced writing projects (e.g. complex clinical study reports, protocols, more challenging indications, or customers). Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. May provide feedback to peers when...

Summary of Position: - Alcon is looking to hire Medical Safety Writer to join our Medical Safety Writing team at Bengaluru in India. This role will Support Global Medical Safety in preparation of regulatory safety documentation and ensure the safety documents comply with applicable standards and regulations across region_ Key Responsibilities: - Act as...

**Job Title**:Associate Medical Writer. **About the department** Global Medical Affairs, GBS (GMA GBS) is an extension of the Global Medical Affairs unit in Headquarters (HQ) in Denmark and is based out of Global Business Services (GBS), Bangalore, India. One of the team within GMA-GBS is Medical Affairs department including a sub-team for marketed...

Summary of Position: - Alcon is looking to hire Medical Safety Writer to join our Medical Safety Writing team at Bengaluru in India. This role will Support Global Medical Safety in preparation of regulatory safety documentation and ensure the safety documents comply with applicable standards and regulations across region_ Key Responsibilities: - Act as...

Job Description:Job Title: Medical WriterJob description:Prepare, review, and edit reports, manuscripts, drug monographs, medico-marketing material, systematic reviews, and meta-analysis on varied disease domainsPrepare, review, and edit reports on disease background, epidemiology, outcomes and disease burden in oncology and non-oncology domainsHandle...

About thejobAt ICON its our people thatset us apart. Our diverse teams enable us to become a betterpartner to our customers and help us to fulfil our mission toadvance and improve patients lives.Our Own Itculture is driven by four key values that bring us together asindividuals and set us apart as an organisation: AccountabilityDelivery Collaboration...