Principal Medical Writer Jobs in India

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.A Day in the LifeResponsibilities may include:MBBS/MD/ DM/ BDS...

We are looking for a pharmacovigilance medical writer to join our team. The  Medical Writer will be responsible for medical writing including:PSURs/PBRERsPADERsACOsDSURsRMPsQC and review of all written output from the operations team as requiredSupporting the project managers to determine scheduling...

We are looking for a pharmacovigilance medical writer to join our team. The  Medical Writer will be responsible for medical writing including:PSURs/PBRERsPADERsACOsDSURsRMPsQC and review of all written output from the operations team as requiredSupporting the project managers to determine scheduling...

Job Overview:The Medical Writer supports client engagements and internal requests projects and business development efforts by doing the necessary research data collection analysis and interpretation; development of value messages dossiers reports and other written deliverables modeling educational...

Team: Clinical ReportingLocation : Bangalore Novo Nordisk Global Business Services (GBS) IndiaYour New RoleAs a Medical Writer you will perform a wide range of medical writing tasks to support clinical development programs delivering high-quality content and documents that align with the Clinical R...

Introduction:Xencor is a public clinical-stage biopharmaceutical company located in the Los Angeles area (Pasadena) and in San Diego. Our focus is developing high-potential XmAb bispecific T-cell engagers and additional engineered drug candidates that leverage our differentiated technology platforms...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

Position - Manager -Medical WriterDepartment - Medical Affairs Job Responsibilities:Designing of preclinical studies as per the regulatory requirements to support the clinical bridging.Preparation and review of preclinical study synopsis study protocol and reports.Preparation and Review of clinical...

Department: Safety Medical Writing Safety Surveillance Global Patient Safety.Location :Novo Nordisk Global Business Services (GBS) Bangalore IndiaAre you passionate about ensuring patient safety through meticulous scientific writing Do you have the expertise to handle complex safety surveillance re...

Total Experience -3 YearsDepartment: Medical Affairs / Scientific CommunicationsEducation: MBBS / BDS / PhD / Masters in Pharmacy or a related fieldScope: GlobalRole Objective / PurposeTo develop high-quality scientific content and documentation across therapeutic areas by conducting in-depth litera...

Work Flexibility: HybridWhat will you do:Conduct systematic literature searches using scientific databases and search tools.Critically analyze and summarize clinical data from published literature and other scientific sources.Develop literature search protocols screening strategies and documentation...

We are looking for an enthusiastic Associate Medical Writer to join our team (Clan-AP) . The successful candidate will support the team in preparing clear accurate and well-structured medical documents including medical safety documents. This is an excellent entry-level opportunity for someone wi...

Location - GurgaonEffectively collect and evaluate data information and input from multiple sources to create a cohesive content strategy for writing projects.Develop abstracts posters slide-decks and manuscripts (complex) from various data sources including clinical study reports protocols etc.Crea...

End-to-end ownership of abstract/congress/manuscript development To liaise with internal and external authors to develop and submit the various pub. vehicles Perform a literature search and prepare the summary of systematic literature search Perform publication planning tasks: Support in...

Job Overview:Responsible for preparation and coordination of complex clinical study protocols and clinical study reports (CSRs) and other documents as needed. Responsible for preparation of submission level documents. Provide review and feedback on documents prepared by the department. Performs the...