518 Scientific Writing Jobs - Page 8

Collaborate with cross-functional teams to ensure seamless clinical development processes. Develop and implement effective monitoring strategies to enhance patient outcomes. Conduct thorough data analysis and interpretation to inform medical decisions. Provide expert guidance on clinical trial design, methodology, and statistical analysis. Ensure compliance with regulatory requirements and industry standards. Foster strong relationships with stakeholders, including investigators, sponsors, and patients. Job Requirements Strong understanding of clinical development principles, practices, and regulations. Excellent analytical, problem-solving, and communication skills. Ability to work effectiv...

Manage and analyze aggregate reporting data to provide insights and recommendations. Develop and implement effective reporting strategies to meet business needs. Collaborate with cross-functional teams to ensure accurate and timely reporting. Identify and mitigate risks associated with reporting processes. Develop and maintain relationships with stakeholders to ensure effective communication. Stay up-to-date with industry trends and best practices in aggregate reporting. Job Requirements Strong understanding of aggregate reporting principles and methodologies. Experience with data analysis and interpretation to inform business decisions. Excellent communication and interpersonal skills. Abil...

Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols and procedures. Conduct site feasibility assessments and coordinate with investigators. Develop and maintain relationships with key stakeholders, including sponsors and regulatory agencies. Ensure compliance with regulatory requirements and company policies. Participate in risk assessment and mitigation strategies for clinical trials. Job Requirements Strong knowledge of clinical trial regulations and guidelines. Excellent communication and interpersonal skills. Ability to work effectively in a fast-paced environmen...

Roles and Responsibility Manage and analyze aggregate reporting data to provide insights and recommendations. Develop and implement effective reporting strategies to meet business needs. Collaborate with cross-functional teams to ensure accurate and timely reporting. Identify and resolve issues related to reporting data quality and integrity. Develop and maintain complex reports using various reporting tools and technologies. Provide expert guidance on reporting best practices and standards. Job Requirements Strong understanding of aggregate reporting principles and methodologies. Proficient in analyzing large datasets and providing actionable insights. Excellent communication and interperso...

Hiring for Clinical Safety Physician in Mumbai, Bangalore & Noida Any MBBS/MD with min 5 yrs of relevant Exp in Drug Safety, ICSR, Aggregate reporting, Clinical Study Salary up to 25 LPA Call Suhani- 9911988552, Rukhsar-9899875055, Shruti-9911988551

Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols, procedures, and study designs. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate in protocol development and review processes. Job Requirements Minimum 4 years of experience in clinical trials or a related field. Strong knowledge of clinical trial principles, practices, and regulation...

Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols, procedures, and study designs. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate in protocol development and review processes. Job Requirements Minimum 2 years of experience in clinical trials or a related field. Strong knowledge of clinical trial principles, practices, and regulation...

Job title : Sr. Associate HEVA (Evidence Synthesis) Hiring Manager: Head/Group Lead/Research Lead/Team Lead HEVA Location: Hyderabad % of travel expected: Travel required as per business need Job type: Permanent and Full time About the job Sanofi Global Hub is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. MedHub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally. Main responsibilities: The overall purpose and main responsibilities are listed be...

Our Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. SBO strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally. Main responsibilities: The overall purpose and main responsibilities are listed below: To create specialized content with limited supervision; support end-to-end publication/medical education content development process including documentation and approval in PromoMats/iEnvision (previously-Datavision/MATRIX); develop an...

Main responsibilities: The overall purpose and main responsibilities are listed below: To create complex and specialized content without supervision; manage end-to-end publication/medical education content development process including documentation and approval in PromoMats/iEnvision (previously- Datavision/MATRIX); develop and maintain therapeutic area expertise; coach and review content created by junior scientific writers; work in close collaboration with peers/team to develop best practices; and collaborate effectively with stakeholders People: (1) Maintain effective relationship with the end stakeholders (medical scientific community) within the allocated Global Business Unit and produ...

Our Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions . SBO strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally. Main responsibilities: The overall purpose and main responsibilities are listed below: To create complex and specialized content without supervision; manage end-to-end publication/medical education content development process including documentation and approval in PromoMats/iEnvision (previously- Datavision/MATRIX); de...

Our Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization setup tocentralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, andR&D, Data & Digital functions . SBO strives to be a strategic and functional partner for tactic al deliveries to Medical, HEVA, andCommercial organizations in Sanofi, Globally . Main responsibilities: The overall purpose and main responsibilities are listed below: To c reate specialized content with limited supervision ; support end-to-end publication/medical education content development process including documentation and approval in PromoMats/ iEnvision (previously- Datavision/MATRIX ) ; d ev...

Main responsibilities: Responsible for research and authoring of scientific response documents under the direction of the Global Medical Information (GMI) team in support of global and local medical information activities. Responsible for the execution of activities as required in alignment with GMI colleagues. Achieved through a combination of product knowledge, along with editing, writing, and document management proficiency. Essential Job duties and responsibilities: Conducts literature searches and reviews, and extracts/summarizes complex data from the scientific literature. Generates evidence-based, accurate, current, and fair-balanced summaries of data for the creation/maintenance of s...

We are looking for a highly skilled and experienced Clinical Trial Medical Advisor to join our team at Gratitude India Manpower Consultants Pvt. Ltd., with 32 years of experience in the IT Service & Consulting industry. Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols and procedures. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate ...

We are looking for a highly skilled and experienced Clinical Research Medical Advisor to join our team at Gratitude India Manpower Consultants Pvt. Ltd., located in the IT Service & Consulting industry. The ideal candidate will have 2-49 years of experience. Roles and Responsibility Collaborate with cross-functional teams to design and implement clinical research studies. Provide medical expertise and guidance on study protocols, case report forms, and investigational reports. Develop and maintain relationships with investigators, site staff, and other stakeholders. Review and approve study-related documents, including protocols, informed consent forms, and case report forms. Ensure complian...

We are looking for a skilled Medical Writer to join our team at Gratitude India Manpower Consultants Pvt. Ltd., with 2-4 years of experience in the IT Service & Consulting industry. Roles and Responsibility Develop high-quality medical content for various platforms, including reports and presentations. Conduct research and analyze data to create accurate and informative medical documents. Collaborate with cross-functional teams to ensure timely delivery of projects. Edit and proofread medical content for clarity, grammar, and punctuation. Stay updated with industry trends and developments in medical writing. Participate in quality control measures to maintain high standards of medical writin...

We are looking for a highly skilled Medical Writer with 3 to 8 years of experience to join our team in Mumbai. The ideal candidate will have a strong background in medical writing and excellent communication skills. Roles and Responsibility Develop high-quality written materials for various medical publications, including clinical trials and research studies. Collaborate with cross-functional teams to ensure accurate and timely delivery of written content. Conduct thorough research on medical topics and stay updated with the latest developments in the field. Edit and review written content for clarity, grammar, and style. Ensure compliance with regulatory requirements and industry standards....

We are looking for a highly skilled Medical Writer with 2 to 5 years of experience to join our team in Mumbai. The ideal candidate will have a strong background in medical writing and excellent communication skills. Roles and Responsibility Develop high-quality written materials for various medical publications, including clinical trials and research studies. Collaborate with cross-functional teams to ensure accurate and timely delivery of written content. Conduct thorough research on medical topics and stay up-to-date with industry developments. Edit and proofread written content for clarity, grammar, and punctuation. Meet deadlines and deliver high-quality work under tight timelines. Parti...

Data Search & Analysis on the drug discovery and development Creating technology reports Kindly provide minimum two references with resume Required Candidate profile Keen interest in drug discovery, API Good Knowledge of organic chemistry Good Communication Skills

Roles and Responsibility Develop comprehensive, accurate, and engaging medical documents, including reports, articles, and presentations. Collaborate with cross-functional teams to ensure timely delivery of projects and meet deadlines. Conduct thorough research on various medical topics to stay updated with industry developments. Edit and proofread written content for clarity, grammar, and punctuation accuracy. Participate in brainstorming sessions to generate new ideas and concepts for content creation. Stay current with industry trends and advancements in medicine and healthcare. Job Requirements Minimum 5 years of experience in medical writing or a related field. Strong understanding of m...

Roles and Responsibility Conduct thorough reviews of medical records, including patient histories and treatment plans. Analyze data to identify trends and patterns that inform medical decisions. Collaborate with cross-functional teams to develop and implement effective treatment plans. Develop and maintain accurate and up-to-date documentation of review findings. Stay current with industry developments and advancements in medical research. Provide expert guidance on medical matters related to project development. Job Requirements Strong understanding of medical terminology and concepts. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment a...

Roles and Responsibility Develop high-quality medical writing content for various reports, including aggregate reports on pharmacovigilance. Conduct thorough research and analysis to ensure accuracy and completeness of written content. Collaborate with cross-functional teams to gather information and insights for report development. Create engaging and informative content that meets the needs of stakeholders and audiences. Edit and review content for clarity, grammar, and style. Stay up-to-date with industry trends and developments in pharmacovigilance and aggregate reporting. Job Requirements Minimum 2 years of experience in medical writing, preferably in the IT Service & Consulting industr...

Roles and Responsibility Develop high-quality written materials for various medical publications, including clinical trials and research studies. Collaborate with cross-functional teams to ensure accurate and timely delivery of written content. Conduct thorough research on medical topics and stay up-to-date with industry developments. Edit and proofread written content for clarity, grammar, and punctuation. Meet deadlines and deliver high-quality work under tight timelines. Participate in quality control processes to ensure consistency and accuracy in written materials. Job Requirements Strong knowledge of medical terminology and concepts, including anatomy, physiology, and pharmacology. Exc...

Roles and Responsibility Develop high-quality medical reports and documents for pharmaceutical companies. Conduct thorough research on various medical topics related to Pharmacovigilance. Collaborate with cross-functional teams to ensure timely delivery of projects. Analyze complex data sets to identify trends and patterns. Prepare presentations and visualizations to communicate findings to stakeholders. Stay updated with industry developments and regulatory requirements. Job Requirements Minimum 2 years of experience in medical writing, preferably in the IT Service & Consulting industry. Strong knowledge of Pharmacovigilance and Aggregate Reporting. Excellent writing and communication skill...

Roles and Responsibility Develop high-quality medical writing content for various reports, including aggregate reports on pharmacovigilance. Conduct thorough research and analysis to ensure accuracy and completeness of written content. Collaborate with cross-functional teams to gather information and insights for report development. Create engaging and informative content that meets the needs of stakeholders and audiences. Edit and review content for clarity, grammar, and style. Stay up-to-date with industry trends and developments in pharmacovigilance and aggregate reporting. Job Requirements Minimum 4 years of experience in medical writing, preferably in the IT Service & Consulting industr...