538 Medical Writing Jobs

Medical Report Typist - Part Time/Full time Location: Indira Nagar Bangalore Role: Medical Writer Industry Type: Medical Services / Hospital Department: Research & Development Employment Type: Full Time, Permanent Role Category: Pharmaceutical & Biotechnology Education UG: Graduation Not Required, Any Graduate PG: Post Graduation Not Required, Any Postgraduate

We are looking for experienced and dynamic Team Lead in Medical Affair for Oncology to actively contribute to the organization/business by taking people managerial responsibility and being responsible for the scientific, technical and ethical soundness of all policies, statements and endeavours. He/she will need to provide high quality and timely service in the areas of product commercialization/promotional support, interactions with healthcare professionals, continuing medical education, clinical research, sales force training, medical information, and performance/people management, and business support in the areas of new product development, regulatory affairs, quality standards, and information technology; alliance management may be included as applicable. Roles & Responsibilities You will be responsible to provide tactical and strategic inputs, and business/technical expertise, to Product Management towards ethical promotion of assigned products, in the operational areas listed You will be responsible for providing strategic inputs for marketing and brand plans, overseeing the design and execution of medical-marketing programs, and facilitating interactions with healthcare professionals. Additionally, you will initiate, review, and approve promotional and educational materials while ensuring compliance with relevant SOPs, regulations, and industry codes. You will be responsible for developing, reviewing, and approving protocol documents and supporting materials for various clinical projects. Additionally, you will collaborate with Global Medical Affairs and Clinical Development, organize training sessions for project teams, and provide medical support for safety reporting and ongoing local studies. Furthermore, you will contribute to the planning and execution of Investigational New Drug Applications (NDAs). You will be responsible to provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external customers. You will be responsible for training the Sales Force on basic sciences/assigned products and pre-launch and launch training for new products. You will assist the New Product Planning team in preparing business cases and pre-commercialization programs for global products, development of local formulations and line extensions. Additionally, you will provide support in market research, stakeholder mapping, and early access programs. You will also collaborate with various departments to evaluate commercial opportunities, including licensing, acquisitions, and co-promotion. You will be responsible for providing medical and product expertise in the registration of new products/indications, as well as defending marketed products to various stakeholders. You will also oversee the writing and review of labelling documents and provide medical support for the processing of adverse event reports, adhering to relevant SOPs and practices. You will be responsible to develop and share expertise in identified medical and/or scientific therapeutic area, including but not limited to disease areas, markets, products (DRL products and key competitors) and services. You will be responsible to develop and share expertise in a specific medical/scientific subject, including protocol design, development, and training, Pharma co economics, Outcomes Research, Health Technology Assessment, New Product Evaluation, Disease Management Programs, Intellectual Property Protection and Patents, and Medical Information You will be one-point Medical Affairs contact for Customer Relationship Management and operational liaison in the various functional domain. You will be responsible for fostering a culture of learning and development and managing the Medical Affairs staff, providing training, guidance, and support across various functional domains, ensuring adherence to company values and behaviours, and. You will be responsible to support cluster Head Medical Affairs in budgeting, provisioning and expense control. Qualifications Educational Qualification- Post-graduate degree in Pharmacology or other Medical speciality/ Graduate degree in Medicine Minimum work experience -6 to 8 years of relevant experience as Medical Advisor and minimum of 3 years in Oncology Therapy Area. Have prior experience of New Launch in Oncology TA Skills & attributes Technical Skills Basic knowledge of pharmaceutical industry, drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines Knowledge of pharmaceutical medicine including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics and relevant Therapeutic Area/Products Expertise in clinical trial design and methodology, and understanding of interfaces, and conduct Behavioural Skills Communication skills, both written and verbal (including medical writing and presentation skills) Analytical skills and reasoning, and sound medical judgment/decision making Interpersonal skills, internal & external networking and the ability to impact and influence.

We are looking for an experienced Medical Advisor to provide the scientific foundation for the Therapeutic Area (TA) medical strategy, including managing various medical activities and engaging key thought leaders. Oversee the execution of the medical affairs plan, facilitate the flow of medical developments to the sales and marketing team, and contribute to the development of the Medical Affairs strategic plan for identified Therapeutic Area (TA) and products. Roles & Responsibilities You will be responsible for serving as a core scientific member of the cross-functional franchise team, providing the scientific foundation for the Therapeutic Area (TA) medical strategy. You will be responsible for conceptualizing and managing a wide range of medical activities, aligned with the TA Medical strategy, including research, publications, medical education, and patient support programs. You will be responsible for engaging key thought leaders through medical affairs activities, in line with the overall strategic plan. You will be responsible for ensuring the optimal execution of the strategic medical affairs plan through Regional Medical Affairs, encompassing medical education, product education, and special projects. You will be responsible for acting as a therapeutic area scientific expert, discussing scientific data with leading specialists, and providing training on the latest medical developments to the sales and marketing team. Qualification Educational qualification- MBBS with M.D. Pharmacology/Medicine or full time post-graduate qualification in any discipline of medicine Minimum work experience - 2-4 years of experience in the pharmaceutical industry or research company in a Medical Advisor capacity. Skills & attributes Technical Skills Training in medical writing, clinical trial methodologies, research design and ICH GCP will be added advantage Must have working knowledge of Indian regulations pertaining to Health care professional's interactions (MCI code of ethics for doctors & UCPMP Code for Pharma) and Drugs and Cosmetic Act regulations pertaining to clinical trials and new drug approvals Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data Strategic mind set with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship is essential Experience with complex business environments preferred Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards Behavioural Skills Integrity driven decision making skills Sound scientific knowledge Collaboration and teaming with ability to work in a matrix environment Strategic thinking & sound analytical skills Intellectual curiosity Self-awareness and adaptability to work in a matrix environment Result oriented and performance driven Excellent interpersonal & communication skills to effectively interact with a broad range of audience

The Sanofi Business Operations team in India centralizes processes to support various functions within Sanofi globally, such as Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. The team aims to be a strategic partner for Medical, HEVA, and Commercial organizations. As a member of the Medical regulatory writing team, your main responsibilities will include developing medical expertise in regulatory writing, ensuring compliance with FDA, EU, and other regulatory requirements, supporting activities related to marketing authorizations, and collaborating with Global Medical Leads and other departments. Key job duties and responsibilities include providing medical assessments, drafting strategic documents, writing key medical/clinical parts of Common Technical Documents, reviewing compassionate use requests, delivering high-quality medical documents, and collaborating effectively with stakeholders. You will be expected to maintain effective relationships with stakeholders, interact with medical and pharmacovigilance departments, and assist in developing knowledge and sharing expertise within the team. Additionally, you should ensure deliverables are supported as per timelines and quality standards, provide medical strategic insights, and act as an expert in medical regulatory writing. The ideal candidate will have 5 years of experience in supporting international pharmaceutical companies, soft skills including stakeholder management and communication, technical skills in medical operational excellence and editing, a Medical degree (MBBS; MD), and excellent knowledge of the English language. Join the Sanofi team to pursue progress, discover extraordinary achievements, and contribute to better medications and outcomes through collaboration and innovation. Apply now and be a part of a diverse and inclusive team dedicated to making miracles happen.,

Are you passionate about healthcare content creation and possess a degree in healthcare (dentistry/pharmacy/nursing/ayush) Do you aspire to contribute significantly to the EdTech sector for medical professionals If so, an exciting opportunity awaits you to be a part of our Australian healthcare EdTech team as a Content Writer Intern and embark on a journey of growth and development. Our organization is a global healthcare EdTech platform that provides online courses designed to empower a wide range of healthcare professionals including pharmacists, doctors, physiotherapists, nurses, optometrists, dentists, and others to excel on an international level. In this role as a Web Content Writer Intern, you will be responsible for crafting compelling and SEO-optimized content aimed at educating and inspiring healthcare professionals globally. The internship duration is set at 3 to 4 months, with the possibility of a full-time position being extended to high performers upon successful completion of the internship. Eligibility requirements for this position include holding a degree in Dentistry, Pharmacy, or another relevant field. Both freshers and individuals with up to 3 years of content writing experience are welcome to apply. A keen interest in medical writing and digital content creation is essential to thrive in this role. Your responsibilities as a Content Writer Intern will involve creating clear and informative content for healthcare courses, drafting engaging blogs, articles, and research-based educational material, developing impactful social media and video script content for platforms such as YouTube and Reels, implementing SEO best practices to enhance web visibility, and collaborating with the content and marketing teams to deliver content that adds value. We are seeking candidates with excellent English writing and editing skills, a dedication to simplifying complex healthcare topics, strong research capabilities, meticulous attention to detail, a creative mindset, and the ability to take initiative. An understanding of healthcare systems, exams, or professional pathways would be considered a valuable asset. Join us in revolutionizing healthcare education through innovative content creation and contribute to the success of medical professionals worldwide.,

Job Description: As the Director of Safety Writing at GSK, you will be leading the safety writing team to ensure the accurate, clear, and compliant preparation of Aggregate Reports and Risk Management Plans. Your role will involve a deep understanding of regulatory guidelines, effective leadership skills, and the ability to build a best-in-class capability to achieve organizational business goals related to safety writing. You will oversee the efficient preparation of high-quality safety writing deliverables that are strategically aligned and lead a global team of medical writers. Additionally, you will be responsible for optimizing internal and external resourcing, ensuring compliance, implementing best practices, fostering innovation, streamlining processes, and upholding standards of medical writing. Collaboration with the Head of Medical Writing to develop and drive departmental strategies will also be a key aspect of your role. Your leadership will be instrumental in aligning safety writing capabilities with business and operational needs, working closely with cross-functional safety teams for project clarity, and delivering high-quality safety documents that meet regulatory standards. Key Responsibilities: - Take accountability for all safety writing deliverables produced by the Medical Writing function. - Lead change initiatives to operate at the forefront of operational excellence. - Manage and lead line reports, including aspects of personnel management such as hiring, training, professional development, performance evaluations, compensation recommendations, promotions, teambuilding, and supervision of adherence to departmental procedures and health authority regulations. - Define and execute recruitment strategies to attract top talent. - Incorporate organizational considerations into strategic and operational decisions. - Create a compelling future vision and ensure it is measurable and aligned with organizational goals. - Demonstrate a track record of quality decision making and innovative problem resolution with significant operational impact. - Lead initiatives for process improvement, training, quality enhancement, and compliance. - Act as an industry thought leader, providing consultancy in areas like process improvement, pharmaceutical standardization, and implementation of regulatory guidelines. - Cultivate beneficial partnerships with external organizations to meet company objectives. - Oversee the identification and engagement of third-party partners, ensuring their performance and compliance meet business requirements. Basic Qualifications and Experience: - Minimum requirement of a master's degree in Life Sciences/Health or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.). A degree in Medicine/Dentistry/Physiotherapy/Experimental Medicine with patient exposure in a hospital-based setting is advantageous. - A total of 18+ years of experience, with at least 10 years in safety writing within the pharmaceutical industry or a large Contract Research Organization, demonstrating leadership skills. Ideal candidates will have expertise in applying FDA, EU, and ICH guidelines for pharmacovigilance in clinical trials and post-marketing, serving as an internal and external safety writing expert. - Experience working in matrix/multicultural environments and diverse settings, especially within hybrid teams. - Strong negotiation skills for proposing creative solutions to new challenges. - Strategic acumen with robust planning and organizational capabilities. - Proficiency in both written and spoken English. - Ability to mentor and discern essential information, ensure logical flow, clarity, accuracy, and appropriateness for target audiences, such as regulatory authorities. Inclusion at GSK: At GSK, we are committed to inclusion and encourage candidates to reach out if they require any adjustments during the recruitment process. Contact our Recruitment Team at IN.recruitment-adjustments@gsk.com to discuss your needs. Why GSK: GSK is a global biopharma company focused on uniting science, technology, and talent to combat disease collectively. Our mission is to positively impact the health of billions of people and deliver sustainable shareholder returns. We value our people as the cornerstone of our success, striving to create an environment where individuals can thrive, grow, and contribute to our shared ambition of getting ahead of disease together. Important Notice to Employment Businesses/Agencies: GSK does not accept referrals from employment businesses/agencies concerning vacancies posted on this site without prior written authorization. It is essential for employment businesses/agencies to contact GSK's commercial and general procurement/human resources department for authorization before referring any candidates. Unauthorized actions by employment businesses/agencies will not be recognized as having consent or contractual agreement with GSK, and GSK will not be liable for any fees arising from such actions. If you receive unsolicited emails or job advertisements from email addresses not ending in gsk.com, please disregard them and notify us at askus@gsk.com for verification of the job's legitimacy.,

As a Senior Medical Writer at Syneos Health, you play a vital role in leading the clear and accurate completion of medical writing deliverables. Your responsibilities include managing medical writing activities associated with individual studies, coordinating these activities within and across departments with minimal supervision. You will be responsible for completing various documents such as clinical study protocols, reports, patient narratives, annual reports, and more. Adhering to established regulatory standards, including ICH E3 guidelines, company standard operating procedures, and client standards, is essential. Your role involves coordinating quality and editorial reviews, ensuring proper management of source documentation. As a peer reviewer for the internal team, you will ensure document scientific content, clarity, overall consistency, and proper format. Interacting and building good working relations with clients, department heads, and peers in various departments are crucial for producing high-quality writing deliverables. In addition to these responsibilities, you will mentor and lead less experienced medical writers on complex projects, developing deep expertise on key topics in the industry and regulatory requirements. Working within budget specifications for assigned projects while maintaining a high level of quality is a key aspect of your role. To qualify for this position, you should have a Bachelor's degree in a relevant discipline with relevant writing experience, while a graduate degree is preferred. 4-5 years of relevant experience in a disclosure platform and strong understanding of FDA and ICH regulations are necessary. Proficiency in MS Office, strong project and time management skills, and a good grasp of medical terminology and principles of clinical research are also required for this role. At Syneos Health, you will have the opportunity to work in a dynamic and challenging environment where you can make a difference. Join us in our mission to accelerate the delivery of therapies and change lives.,

You are a technology-led healthcare solutions provider, driven by the purpose to enable healthcare organizations to be future-ready. You offer accelerated global growth opportunities for individuals who are bold, industrious, and nimble. At Indegene, you can experience a unique career journey celebrating entrepreneurship, guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, visit www.careers.indegene.com. Imagine moving to an exciting role in an entrepreneurial organization without the usual risks associated with it. At this stage of your career where growth and variety are important to you, Indegene invites you to join their journey and grow with them. Indegene provides roles that offer both excitement and reliability, trusting you from day one to deliver global impact, lead teams, and take responsibility for outcomes while being supported and mentored by leaders. As a profitable rapidly growing global organization, Indegene is seeking the best talent for its current phase of growth. Working at the intersection of healthcare and technology, you will have access to global opportunities with fast-track careers, collaborating with a purpose-driven team. This combination promises a truly differentiated experience for you. If this opportunity excites you, apply for the position of Associate Manager / Manager - Regulatory Writing (Clinical) at Indegene. **Experience:** You should have 10 to 12 years of experience in writing Clinical & Regulatory documents supporting global filings, specifically CTD Module 2 and Module 5. **Role Purpose:** Your role involves handling complex Medical Writing projects, providing review support for medical writing deliverables that support the clinical regulatory writing portfolio, and training junior writers. **Skills:** - Experience in authoring various clinical document types to support regulatory filings - Lead cross-functional teams to draft scientific/medical content - Understanding of the clinical development process - Effective communication and time management skills - People management experience - Customer focus and ability to work independently - Adherence to structured processes for document delivery - Ability to manage tasks, roles, and responsibilities within the authoring team - Strong knowledge of regulatory guidelines and regional requirements - Ability to interpret data and apply scientific knowledge to support regulatory document writing - Comfortable working on cross-functional teams **Knowledge Requirement:** - Strong scientific knowledge - Understanding of regulatory guidelines/requirements - Ability to interpret data and apply scientific knowledge - Manage messaging for consistency and alignment with strategy **Technology Skills:** - Expert authoring in MS Word - Experience working in document management systems - Capable of training writers/authors on the use of templates and tools **Responsibilities:** Prepare/review clinical study reports without guidance from senior members of the writing staff.,

As a Manager, Medical Writing & Research Affairs at TECCRO, you will play a crucial role in preparing high-quality scientific documents, including clinical study reports, research papers, regulatory submissions, and publications for medical journals. Your responsibilities will involve collaborating closely with clinical and research teams to ensure that manuscripts meet publication standards for major medical journals and align with the latest scientific research and TECCRO's clinical objectives. Your role will also require you to conduct thorough literature reviews, contribute to the design of clinical trials, and stay updated with current scientific and clinical advancements in the fields of medical aesthetics, skincare, and clinical trials. Additionally, you will work closely with internal teams, including clinical researchers, data managers, and regulatory affairs, to support the alignment of documents with clinical objectives and regulatory standards. Your expertise in medical writing will be essential for supporting business development efforts, including proposal creation and client communication. You will also assist in the preparation of regulatory submissions, ensuring that scientific documents align with required formats and regulatory guidelines. To excel in this role, you should possess exceptional writing, editing, and proofreading skills with a meticulous attention to detail. A strong understanding of clinical research methodologies, regulatory guidelines, and Good Clinical Practices is required. Proficiency in using writing and reference management software, along with excellent collaboration skills, will be beneficial for effectively working across cross-functional teams. If you are a skilled medical writer with a passion for science and research, this role offers an exciting opportunity to contribute to the advancement of clinical research and academic publications within the growing field of medical aesthetics. TECCRO provides a competitive salary with performance-based incentives, opportunities for professional development, certifications, and career growth, along with a supportive and collaborative work environment focused on research excellence and innovation in clinical trials. Join us at TECCRO and be a part of driving scientific and technological innovation in the aesthetics industry!,

You will be responsible for leading scientific engagement with Medical Experts as the MSL Manager. In this role, you will implement clinical and educational strategies, as well as respond to unsolicited medical inquiries. Your key responsibilities will include building and maintaining scientific relationships with Medical Experts, identifying key accounts aligned with medical priorities, developing engagement plans tailored to country-specific strategies, and providing accurate scientific information in response to medical inquiries. Additionally, you will support clinical trial execution, facilitate Investigator Initiated Trial processes, act as a scientific resource for internal field teams and partners, and ensure timely reporting of adverse events and product complaints. To excel in this role, you must have proven experience in operations management and cross-functional collaboration, a strong understanding of clinical research and medical affairs processes, proficiency in scientific communication including medical writing and data interpretation, familiarity with CRM tools and digital platforms for stakeholder engagement, knowledge of disease management, drug development, and epidemiology, and the ability to analyze and present clinical data effectively. Fluency in English, both written and spoken, is essential. Desirable requirements include prior experience in a Medical Scientific Liaison or similar field-based medical role, as well as an advanced degree in life sciences such as MD, PhD, or PharmD. Novartis is committed to creating an inclusive work environment and diverse teams that represent the patients and communities served. If you require any reasonable accommodation due to a medical condition or disability during the recruitment process, please reach out to [email protected] with the details of your request and the job requisition number. Join Novartis in reimagining medicine to improve and extend people's lives. Be part of a community of smart, passionate individuals collaborating, supporting, and inspiring each other to achieve breakthroughs that positively impact patients" lives. Visit https://www.novartis.com/about/strategy/people-and-culture to learn more about our mission and opportunities.,

Job Description: Manipal Hospitals is seeking a dedicated and detail-oriented Associate Medical Transcriptionist to join our team. The ideal candidate will be responsible for accurately transcribing medical dictations from healthcare professionals, ensuring that all information is documented clearly and comprehensively. This role is essential for maintaining high-quality patient records and supporting our commitment to excellent healthcare service. Key Responsibilities: - Transcribe dictations from physicians and other healthcare providers promptly and accurately. - Review and edit transcriptions for grammar, clarity, and accuracy while ensuring adherence to confidentiality standards. - Familiarize yourself with medical terminology, procedures, and abbreviations to enhance transcription efficiency and precision. - Collaborate with medical staff to resolve any discrepancies or clarify unclear information in transcriptions. - Maintain an organized workflow to ensure timely completion of assignments while meeting deadlines. - Participate in ongoing training to stay updated with industry standards and technological advancements in medical transcription. Qualifications: - A diploma or certificate in medical transcription or a related field. - Strong understanding of medical terminology, anatomy, and physiology. - Excellent typing skills with a high level of accuracy. - Proficiency in using word processing software and medical transcription tools. - Good communication skills and a keen attention to detail. What We Offer: - A dynamic work environment within a leading healthcare organization. - Opportunities for professional growth and development. - A collaborative team atmosphere focused on excellence in patient care. Join Manipal Hospitals and contribute to enhancing patient outcomes through precise and efficient medical transcription. Roles and Responsibilities: - Accurately transcribe medical dictations from healthcare professionals into a written format. - Ensure the correct use of medical terminology, symbols, and abbreviations while transcribing. - Review and edit transcriptions for clarity, grammar, and completeness before final submission. - Maintain confidentiality and adhere to HIPAA regulations regarding patient information. - Collaborate with healthcare providers to clarify any unclear dictations or terms. - Stay updated on the latest medical practices and transcription technologies. - Manage and prioritize workload to meet deadlines in a fast-paced environment. - Utilize transcription software and equipment efficiently to enhance productivity. - Participate in training sessions and professional development opportunities as required. - Assist in quality assurance processes by providing feedback and support to improve transcription accuracy.

As a Scientific Content Writer at our company, your primary responsibility will be to prepare and create high-quality scientific content in compliance with industry standards and company SOPs. You will curate scientific information with precision, ensuring proper formatting and clarity to accurately represent scientific and clinical data while maintaining originality in writing. It will be essential for you to stay informed about industry trends, regulatory changes, guideline updates, and recent medical literature to enhance content quality and include clinically relevant information. Managing timelines and deliverables efficiently will be crucial to uphold the quality of content without compromise. Additionally, you will be tasked with developing surveys, polls, and quizzes across various specialties based on recent updates in clinical practice. To excel in this role, you should ideally possess an M.Sc. or Ph.D. in Life Sciences, or a background in B. Pharm / M. Pharm. Previous experience in medical writing within the pharmaceutical or healthcare sector is preferred. An in-depth understanding of the subject matter and scientific principles will be beneficial, along with proficiency in using Microsoft Office Suite. Your strong project management skills, ability to handle multiple projects, meet deadlines, and adhere to high-quality standards will be critical for success in this position.,

Hiring for Healthcare authorization Need B.pharma & M.Pharma pass with 1yr exp in medical scribe, authorization, summarization Loc Gurgaon Salary upto 5.80LPA 5 Days working Rotational shift/OFF Snehal 9625998099 Lakshita 8595954721 Divya 9910810424 Required Candidate profile Candidates must have Good communication skills. Candidates must be comfortable working in any shifts.

Primary Responsibilities: Review and analyze patient medical records for accurate code assignment Ensure adherence to coding guidelines and regulatory requirements Learn to use medical coding software Apply understanding of anatomy and physiology to interpret clinical documentation and identify applicable medical codes Stay updated on industry changes and attend relevant training sessions Ensure confidentiality and security of all patient information Comply with the terms and conditions of the employment contract, company policies and procedures, and any and all directives (such as, but not limited to, transfer and/or re-assignment to different work locations, change in teams and/or work shifts, policies in regards to flexibility of work benefits and/or work environment, alternative work arrangements, and other decisions that may arise due to the changing business environment). The Company may adopt, vary or rescind these policies and directives in its absolute discretion and without any limitation (implied or otherwise) on its ability to do #NTRQ Required Qualifications: Bachelor’s degree or master’s degree, from a medical science backdrop or anything relevant Life Science or Bioscience, Pharmacy or Pharmaceutical Sciences, Nursing or Medicine Allied Health Good knowledge in medical terminology basics Good knowledge in Anatomy physiology basics Well-versed with ICD-10 guidelines and their implementation Proficient in reviewing medical records and determining the accuracy and completeness of the document Preferred Qualifications: AAPC/AHIMA Certification Risk Adjustment coding experience At UnitedHealth Group, our mission is to help people live healthier lives and make the health system work better for everyone. We believe everyone – of every race, gender, sexuality, age, location and income – deserves the opportunity to live their healthiest life. Today, however, there are still far too many barriers to good health which are disproportionately experienced by people of color, historically marginalized groups and those with lower incomes. We are committed to mitigating our impact on the environment and enabling and delivering equitable care that addresses health disparities and improves health outcomes – an enterprise priority reflected in our mission. External Candidate Application Internal Employee Application

Looking for a motivated individual to join our team as a Trainee Medical Reviewer in Bengaluru. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Conduct thorough medical reviews of patient records and reports to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve issues related to medical review. Develop and maintain expertise in medical terminology, regulations, and guidelines. Provide high-quality support to internal stakeholders through effective communication and documentation. Stay updated with changes in regulations and guidelines affecting medical review processes. Participate in quality improvement initiatives to enhance the efficiency and effectiveness of medical review activities. Job Requirements Strong understanding of medical terminology, regulations, and guidelines. Excellent analytical and problem-solving skills with attention to detail. Ability to work effectively in a team environment and communicate complex information clearly. Proficiency in using electronic health records systems and other healthcare software applications. Strong organizational and time management skills with the ability to prioritize tasks and meet deadlines. Commitment to delivering high-quality results and maintaining confidentiality and professionalism. Omega Healthcare Management Services Private Limited is a leading provider of healthcare management services, committed to delivering exceptional care and customer satisfaction. We are an IT-enabled services company that uses technology to improve healthcare operations and outcomes.

Description Primary Responsibilities: Drafting and/or content QC of Module 2.5 and 2.7 for INDs, NDAs, BLAs and other regulatory submissions. Drafting and/or content QC of clinical sections for Investigators Brochure (IB) and Briefing packages. Drafting and/or content QC of clinical study protocols and Clinical study reports (CSR) Perform Quality Check (QC) of clinical documents for consistency, accuracy of data and content. Assist in gap analysis of regulatory dossier. Verification of comment resolutions and taking up the document for finalization. Secondary Responsibilities: Participate and provide internal training on various technical matters/subjects. Any other responsibilities given by the reporting lead/manager from time to time. Preparation of Standard Operating Procedures and workflow process. Be Audit ready and updated with recent regulatory guidelines. Interactions (With different internal teams/stakeholders/clients/etc.): Communication with other team members during the course of work requirements.

You are a highly skilled and knowledgeable Content Writer responsible for creating, editing, and reviewing high-quality medical content for various platforms. Your audience will include healthcare professionals and the general public, depending on the project's requirements. The ideal candidate will have a strong background in healthcare or life sciences, along with the ability to translate complex medical information into clear, engaging, and accurate content. Your key responsibilities will include being a creative and visionary communications and content professional with expertise in science, health, and medicine. You will develop and lead high-performing teams across different cultures and geographies in a global landscape. Driving high editorial standards for creating quality content with multi-media experience in various settings such as news, magazines, journals, books, websites, and agencies is crucial. You will deliver key engaging messages with maximum impact and strategic advantage through print, digital, and social media channels. As a proficient writer and editor, you will cater your medical writing to the audience and simplify technical information. Your excellent project management skills will be put to use in managing large volumes and multiple projects simultaneously. Additionally, you will be responsible for creating and producing B2B and B2C marketing content, including product brochures, infographics, eDM campaigns, content marketing for thought leadership, surveys and analytical reports, and social media advertising through platforms like TrendMD, Google Adwords, and Facebook. Strong organizational and interpersonal skills are essential for this role. Requirements for this position include a minimum of 4 years of experience in the medical/healthcare field and 5 years in medical writing. Candidates with qualifications such as B Pharm, M Pharm, MD, MBBS, etc., are preferred. This position is based in Mumbai and is a full-time role requiring in-person work. If you are interested in this opportunity, please share your resume at hrc@centrixhealthcare.com. This is a full-time position with a day shift schedule. The ideal candidate should have a total of 4 years of work experience.,

Role: Medical Writer Shift: Rotation Shift Location: Chennai WFO In this role you will be responsible for: Developing high-quality, scientifically accurate medical and regulatory documents, including clinical study reports, protocols, brochures, and more. Creating clear, concise, and audience-appropriate medical content for healthcare professionals, regulatory agencies, and internal stakeholders. Conducting thorough research and literature reviews to ensure content accuracy and compliance with industry standards. Collaborating with subject matter experts, scientists, and regulatory teams to develop compelling and compliant medical writing materials. Adhering to client and regulatory guidelines (e.g., ICH, FDA, EMA) while ensuring consistency, accuracy, and scientific integrity in all documents. Reviewing and revising content based on feedback from reviewers and editors. Managing multiple writing projects simultaneously while meeting strict deadlines and quality standards. Supporting quality control and peer-review processes to ensure excellence in medical documentation. Requirements for this role include: A Bachelors, Masters, or Doctorate degree in Life Sciences, Medicine, Pharmacy, or a related field. 3+ years of experience in medical writing within the pharmaceutical, healthcare, or life sciences industries. Strong understanding of medical and scientific terminology, clinical research processes, and regulatory requirements. Excellent writing, editing, and verbal communication skills with a keen eye for detail. Experience in preparing clinical and regulatory documents, publications, and scientific communications. Ability to interpret and summarize complex scientific data for different audiences. Familiarity with industry guidelines (e.g., ICH, GCP, AMA, FDA, EMA). Proficiency in Microsoft Office Suite and reference management tools. Strong organizational skills, ability to multitask, and work independently under tight deadlines. Experience collaborating with cross-functional teams, including researchers, medical professionals, and regulatory experts.

Consultant - Microbiologist: Mission - The mission of the position of Consultant Microbiologist is to lead operations of the Microbiology Department in Central Laboratory, responsibilities include creating operations plans, managing complete analytical operations, and supervising a team to ensure plans are being executed effectively. Roles & Responsibilities - 1. Technical Operations: Analyze and interpret results from the Microbiology Department with timely verification, approval, and reporting of test results. Collect and analyze abnormalities. Diagnose diseases or study medical conditions using techniques. Ensure all procedures are performed in compliance with NABL guidelines for specimen handling and processing, test analysis, reporting, and maintaining records of patient results. 2. Technical Operations Management (Central Laboratory and Regional Laboratory): Determines technical operational strategies by conducting needs assessments, identifying and evaluating technologies & resources; defining requirements; and establishing technical prerequisite, quality, and service standards. Responsible for making continuous improvements in existing systems, resources, and efficiencies of the Microbiology Department to improve profitability. Oversee and manage day-to-day operational activities/ services and ensure seamless operations across the Microbiology department of Central Laboratory. To establish quality standards, and supervise quality control and operational timelines. Develop and enforce Laboratory Services procedures/policies and ensure their adherence across the assigned department. Establish SOPs and process documentation to ensure a consistent level of service delivery across the organization. To ensure that laboratory operations comply with all rules and regulations to guarantee the highest quality of results. Develop and maintain departmental quality assurance and quality control programs, taking corrective action when indicated. 3, Relationship Management: - To conceptualize and plan medico marketing events and activities with the Sales & Marketing Department for generating revenue for the organization. Collaborate with team members in the development of relevant activities in assigned project(s). Provide consultation to the physicians/ staff/ patients in interpreting test results. Assists in organizing CMEs and Round Table conferences with internal and external stakeholders. Interact with doctors/corporations on a regular basis to ensure quality services and reporting. 4. Communication & Promotion: To conduct regular meetings & circulate the latest scientific information with the help of the Marketing team to internal and external stakeholders. To undertake medical writing for various publications as well as internal purposes and actively collaborate with and support marketing teams for brand promotions. Contributes to the development of promotional materials for the Brand. Provide Medical support to - Marketing and Sales (visual aids, promatograms, clinics i.e. Book, Patient information leaflet, a flowchart of the test, etc.) 5. Training and Development Educate physicians, students, and staff as per identified training needs. To train marketing and field employees on tests, products, and services during onboarding and new product launches relevant to the promotional strategy. Provide training and mentoring to the Dr. B. Lal Institute of Paramedical Sciences Students and Paramedical trainees. Participate in professional organizations or conferences to keep abreast of developments. 6. Research and Development With direct supervision, support, manage, and execute all aspects of research and development-related projects, objectives, and initiatives. Compiles, validates, organizes, and updates research data & findings. Partner with other departments or consulting firms to perform research or other applicable studies or support. Participate and actively engage in all the research and training activities at a laboratory in coordination with the institute 7. People Management: Establish and maintain standards of performance and ensure competency checks at each role in the Operations department. Ensure HR compliance and working as per the HR policy of the organization. Perform monthly Internal review and training of employees at the Microbiology Department or Branch. Lead/contribute to the training, education, and guidance on quality, customer care, and compliance policy/practices.

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases.Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. What are we looking for Drug saftey associate Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualification Bachelor of Pharmacy,Master of Pharmacy

About The Role Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory Senior Analyst Qualifications: BCom Years of Experience: 5 to 8 years Language - Ability: English(Domestic) - Intermediate About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do We help clients address quality and productivity issues, keep pace with customer expectations, navigate regulatory and operational pressures and ensure business sustainability by transforming their banking operations into an agile, resilient operating model.The Corporate banking /Wholesale banking team is responsible for helping clients and organizations processes trade finance transactions by providing superior service delivery to trade customers whilst safeguarding the bank from risks associated with this business.Identify and assess, prevent and mitigate and account to provide reasonable measures to adapt before executing an agreement in relation to the real estate and immovable property. Valuation of commercial real estate using software like Argus, extracting key information from lease agreements (including amendments) and rent rolls. What are we looking for Ability to handle disputesAbility to meet deadlinesAbility to perform under pressureAbility to work well in a teamAdaptable and flexible Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualification BCom

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases.Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. What are we looking for Drug Safety AssociateDrug Safety Associate Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualification Bachelor of Pharmacy,Master of Pharmacy

We are looking for a highly skilled Medical Content Writer with 3 to 9 years of experience to join our team at Digilantern. The ideal candidate will have a strong background in medical writing and excellent communication skills. Roles and Responsibility Develop high-quality, engaging medical content for various platforms. Conduct research and interviews to gather information and insights. Collaborate with cross-functional teams to ensure consistency and accuracy. Edit and proofread content for clarity, grammar, and punctuation. Stay up-to-date with industry trends and developments. Meet deadlines and deliver content on time. Job Requirements Minimum 3 years of experience in medical writing or a related field. Strong knowledge of medical terminology and concepts. Excellent writing, editing, and communication skills. Ability to work independently and as part of a team. Strong research and analytical skills. Familiarity with content management systems and publishing software.

We are looking for a highly skilled and experienced Pharmacist to join our team at MAX Hospital in Noida. The ideal candidate will have 3 to 8 years of experience in the pharmaceutical industry, with a strong background in pharmacy practice. Roles and Responsibility Dispense medications to patients and provide counseling on their proper use. Manage inventory and maintain accurate records of prescriptions and dispensing activities. Collaborate with healthcare professionals to develop and implement medication therapy plans. Conduct patient assessments and monitor their response to medication therapy. Develop and implement pharmacy protocols and procedures. Participate in quality improvement initiatives to enhance patient care and safety. Job Requirements Hold a degree in Pharmacy (D.Pharm, B.Pharm, M.Pharm) from a recognized institution. Possess a minimum of 3 years of experience in pharmacy practice, preferably in a hospital setting. Demonstrate strong knowledge of pharmaceuticals, medications, and medical terminology. Exhibit excellent communication and interpersonal skills. Ability to work effectively in a fast-paced environment and prioritize tasks is essential. Strong analytical and problem-solving skills are required.

About The Role Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do We help clients address quality and productivity issues, keep pace with customer expectations, navigate regulatory and operational pressures and ensure business sustainability by transforming their banking operations into an agile, resilient operating model.The Corporate banking /Wholesale banking team is responsible for helping clients and organizations processes trade finance transactions by providing superior service delivery to trade customers whilst safeguarding the bank from risks associated with this business.Identify and assess, prevent and mitigate and account to provide reasonable measures to adapt before executing an agreement in relation to the real estate and immovable property. Valuation of commercial real estate using software like Argus, extracting key information from lease agreements (including amendments) and rent rolls. What are we looking for Ability to establish strong client relationshipAbility to handle disputes Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualification Any Graduation