169 Scientific Writing Jobs

You will be responsible for understanding the current practices, medicines, and trends in the specific therapeutic area by engaging in doctor visits, attending scientific symposia, and reviewing key therapeutic journals. This information will be crucial for providing relevant insights to both internal and external stakeholders. Your role will also involve publishing scientific articles related to company products and creating presentations for doctors, including those for Continuing Medical Education (CME) and product launches. As part of the team, you will contribute to the implementation of the medico marketing strategy and engage in field visits to doctors for product management purposes, ensuring the development of Key Opinion Leaders (KOLs). You will be entrusted with approving various materials such as Labels (LBLs), Visual Aids (VAs), product monographs, and other medico-marketing content to promote the products effectively. Additionally, you will provide product rationale and clinical data for new products/indications and support regulatory affairs by assisting in the approval of pack inserts (PI) and other medical data. Furthermore, you will be involved in the preparation of Periodic Safety Update Reports (PSURs) and tracking their update dates for the pharmacovigilance process. Your attention to detail and proactive approach will be essential in ensuring compliance and maintaining accurate records.,

Summary As a key contributor within the R&D organization at Hollister Incorporated, the Scientific Communications Writer will play a critical role in transforming complex technical data and research findings into compelling, accurate, and accessible scientific content. This individual will partner with Ostomy Technology Development and cross functional business teams to support the development of technical publications, white papers, abstracts, and internal education materials. The ideal candidate will have strong scientific acumen, data interpretation skills, publications and a solid foundation in statistics and testing methodologies commonly used in medical devices or healthcare research. Responsibilities People & Collaboration Partner closely with cross-functional teams in R&D to understand scientific narratives and translate them into high-quality technical and educational content. Establish and maintain strong relationships with technical experts, product development scientists, and global stakeholders to align messaging with Hollister&aposs scientific and innovation strategy. Collaborate with statisticians, test engineers, and lab scientists to interpret and communicate results from experiments and clinical evaluations. Performance & Execution Deliver timely, scientifically accurate, and well-structured publications, including slide decks, technical white papers, posters, abstracts, and manuscripts for internal and external dissemination. Provide data-driven support for scientific messaging by conducting literature searches, analyzing and summarizing experimental, analytical, or clinical datasets using descriptive and inferential statistics. Review and revise draft materials to ensure data integrity, clarity, consistency, and compliance with applicable scientific and regulatory standards. Process & Methodology Support the scientific communication lifecyclefrom needs assessment through planning, writing, peer review, and submission/presentation. Develop and maintain internal reports and evidence dossiers that summarize the performance and safety of Hollisters products and technologies, incorporating relevant statistical findings and visualizations. Support experimental documentation and reporting in alignment with design control processes, including product testing and method validation summaries. Stakeholder Engagement Collaborate with Ostomy Technology Development teams to ensure that innovation outputs are captured and communicated effectively through internal knowledge-sharing platforms and external publications. Engage with Clinical Education and Marketing to translate technical content into formats that support customer education and training programs. Essential Functions of the Role**: Translate scientific information into technical content by working with cross-functional R&D teams to ensure alignment with Hollisters scientific messaging. Maintain collaborative relationships with subject matter experts to obtain, verify, and clarify technical information for scientific and educational deliverables. Interpret experimental and clinical data through collaboration with statisticians and technical experts to support accurate and meaningful communication. Create scientific publications and communication materials (e.g., slide decks, white papers, posters, abstracts) that clearly and accurately convey technical content for internal and external audiences. Analyze and synthesize data from literature, experimental, and clinical sources to support evidence-based messaging. Ensure quality and compliance of scientific materials through review and revision to meet regulatory, editorial, and scientific standards. Work Experience Requirements Minimum of 4 years of experience in technical/scientific writing, preferably within an R&D or clinical research function in the medical device, pharmaceutical, or healthcare industry. Experience interpreting scientific data and testing results, including familiarity with statistical tools (e.g., Minitab, JMP, Excel, or Python/R for data analysis). Education Requirements Advanced degree (MS/PhD preferred) in a scientific discipline such as biomedical engineering, life sciences, materials science, pharmacy, or related field. Specialized Skills/Technical Knowledge Solid understanding of experimental design, statistical analysis, and data visualization. Ability to translate lab testing and research findings into clear, accurate, and compliant scientific communication. Proficiency in analyzing raw data and summarizing results into scientifically valid conclusions. Soft Skills Strong written and verbal communication skills tailored to both technical and non-technical audiences. Effective stakeholder management and project coordination. Ability to work independently while engaging proactively with cross-functional teams. Local Specifications (English And Local Language) Excellent command of written and spoken English. Location - Gurugram Mode - Hybrid Show more Show less

Position: Research Intern Food R&D (Unpaid) Location: Chennai (Preferred) We are looking for a motivated and detail-oriented Research Intern to join our innovative R&D team. This role is best suited for candidates with a background in Food Technology, Food Science , or related disciplines, and a keen interest in functional ingredients, nutraceuticals, and clean-label innovation. Key Responsibilities Conduct structured literature reviews on functional foods, nutraceuticals, and processing techniques using PubMed, Scopus, and Google Scholar. Analyze scientific data to support R&D decisions and ingredient evaluations. Track market trends in clean-label, sustainable, and health-focused product development. Assist in functionality testing and support formulation for stability, efficacy, and cost-efficiency. Document experimental findings, research outcomes, and lab observations thoroughly. Collaborate with cross-functional teams on formulation, process improvement, and innovation projects. Prepare technical reports, research summaries, and ingredient profiles for internal documentation. Required Qualifications & Skills Pursuing or completed B.Tech/M.Tech/M.Sc in Food Technology, Food Science, or a related field. Strong aptitude in literature review and familiarity with scientific databases/tools. Prior experience with scientific writing or research publications is a plus. Analytical, detail-focused, and scientifically curious. Comfortable working in dynamic, team-oriented R&D settings. Learning Outcomes Practical exposure to end-to-end food R&D processesfrom research to prototype development. Hands-on experience in scientific writing, data interpretation, and technical documentation. Deeper understanding of current consumer and market trends in health and wellness. Collaborative work experience across formulation, regulatory, and innovation teams. Foundational knowledge in food regulations, functional ingredients, and product analysis. Show more Show less

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!,

The role of Scientific Writer Content involves updating or creating scientifically and medically accurate content for commercial and medico-marketing assets such as newsletters, RTEs, civics, social media posts, websites, digital and print brochures, banners, etc. You will be responsible for ensuring that the content for existing or new assets for Novartis Brand or products reflects the most recent changes to Important Safety Information (ISI), Prescribing Information (PI), and other reference documents. It is essential that these updates are consistent with the stringent MLR guidelines and specifications (Medical-Legal-Regulatory). As a part of the "Creative" team under Centralized Asset Support Team (CAST), you will need to demonstrate strong collaboration with colleagues across all Novartis sites in India, the US, Ireland, and Mexico. Operating in a metricized environment, maintaining the highest quality standards, and embodying Novartis values and behaviors daily are also key aspects of this role. The key responsibilities of this position include developing and reviewing scientifically accurate, engaging, and compliant promotional materials like iCVAs, brochures, digital campaigns, emails, social media posts, banners, etc. You will ensure that the messaging is consistent with brand strategy and aligned with approved product positioning. Additionally, you will partner with cross-functional teams to plan and execute content strategy across different platforms, supporting omnichannel content planning and contributing to modular content models. Monitoring and interpreting label updates, ensuring timely content revision across all promotional assets, and liaising with editorial, creative, and regulatory teams to maintain alignment with the latest approved label are also crucial responsibilities. In terms of qualifications, an advanced degree in life sciences, pharmacy, medicine, or a related field is required, along with at least 7 years of experience in scientific writing focusing on promotional material, content planning, and label updates. A deep understanding of promotional scientific communications, clinical data interpretation, pharmaceutical regulations, and familiarity with promotional content review systems and relevant codes are necessary. Strong strategic thinking abilities, excellent communication skills, and the capacity to work cross-functionally in a matrix environment with high attention to detail and timelines are also essential. Exposure to global content localization/adaptation, understanding of omnichannel marketing, and familiarity with modular content are additional advantageous qualifications. Novartis is committed to fostering an outstanding, inclusive work environment with diverse teams that are representative of the patients and communities served. The company is also dedicated to working with individuals with disabilities and providing reasonable accommodations. If you require an accommodation due to a medical condition or disability during the recruitment process or to perform essential job functions, please contact diversityandincl.india@novartis.com. Novartis offers a collaborative community of smart, passionate individuals dedicated to making a positive impact in patients" lives through innovative science. If you are ready to contribute to creating a brighter future together, consider joining the Novartis team. To explore potential career opportunities at Novartis, you can sign up for the talent community to stay connected and informed about suitable roles as they become available. For more information about the benefits and rewards Novartis provides to help employees thrive personally and professionally, please refer to our handbook: https://www.novartis.com/careers/benefits-rewards.,

As a Technical Writer in the Pharmaceutical, Life Science, and Clinical domain with 4-6 years of experience, you will be joining as an immediate joiner under the Contractual Work mode. The position allows remote work. You will be responsible for creating engaging and informative content related to medical and pharmaceutical topics across various platforms like websites, blogs, scientific publications, and marketing materials. Your role will involve collaborating with subject matter experts and researchers to simplify complex medical and pharmaceutical concepts into easily understandable content. Your primary responsibilities will include developing a wide array of medical and pharmaceutical content such as scientific articles, blog posts, whitepapers, research summaries, patient education materials, and marketing collateral. You will be expected to conduct thorough research on medical and pharmaceutical subjects to ensure the accuracy and credibility of the content. It is crucial to adhere to industry-specific regulations and guidelines like FDA and EMA when creating content related to pharmaceutical products and healthcare services. Your role will also focus on engaging various audiences including healthcare professionals, patients, and stakeholders with different levels of expertise. Collaborating closely with subject matter experts, healthcare professionals, researchers, and marketing teams will be essential to gather necessary information and insights for content development. Implementing meticulous proofreading and editing processes will be necessary to maintain high quality and accuracy in all written materials. Moreover, your contribution to content strategy development by identifying key topics, trends, and audience preferences in the medical and pharmaceutical field will be vital. You will also be responsible for optimizing content for search engines to improve its visibility and reach.,

Summary To write, support and manage projects to prepare high quality medical and scientific communications including, literature review, abstracts, posters, slide sets, Manuscripts (complex) for publication/ presentation at congresses or internal medical and/or clinical team, About The Role Location Hyderabad Hybrid Major Responsibilities Prepares, literature review, abstracts, posters, and slide sets, and Manuscripts (complex) working from various data sources including clinical study reports, patient profiles, protocols etc Performs quality control (QC) checking / proof reading of the above-mentioned deliverables to meet customer expectations, Manages multiple projects of up to two brands at any given time, Obtains feedback from customers and implements customer management tactics Complies with and support groups project management tool, standards, policies and initiatives, Follows Novartis specifications for documentation, specifically Novstyle, templates etc Follows and tracks clinical trial milestones for assigned projects, Maintains records for all assigned projects including archiving, Maintains audit, SOP and training compliance Train new joiners, fellow colleagues as and when required Performs additional tasks as assigned, Minimum Requirements Minimum Education Science degree or equivalent, B Sc /equivalent with 8 years Clinical Research (CR) experience, M Sc /M Pharm +6 years of clinical research (CR) experience, Desired Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent), PhD + 4 year of CR experience, MBBS/equivalent + 4 year of CR experience, MD +2 years of CR experience, Why Novartis: Our purpose is to reimagine medicine to improve and extend peoples lives and our vision is to become the most valued and trusted medicines company in the world How can we achieve thisWith our people It is our associates that drive us each day to reach our ambitions Be a part of this mission and join us! Learn more here: https:// novartis / about / strategy / people-and-culture Youll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook https:// novartis /careers/benefits-rewards Commitment To Diversity And Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve, Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork novartis /network, Why Novartis: Helping people with disease and their families takes more than innovative science It takes a community of smart, passionate people like you Collaborating, supporting and inspiring each other Combining to achieve breakthroughs that change patientslives Ready to create a brighter future togetherhttps:// novartis / about / strategy / people-and-culture Join our Novartis Network: Not the right Novartis role for youSign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork novartis /network Benefits and Rewards: Read our handbook to learn about all the ways well help you thrive personally and professionally: https:// novartis /careers/benefits-rewards Show

Roles and Responsibilities Candidate will be required to do desk research on various domains like English Literature, Social Science and Management and write academic content related to the same. Content in the form of scientific papers, research articles, review papers and literature review will need to be written. Knowledge of systematic literature review, APA citation style, Harvard referencing system would be an added advantage. Desired Candidate Profile An ideal candidate will be a MBA, PGDM, Master's in Marketing, Finance, HR, Project Management, Operations Management, or English Literature with excellent English writing skills. Desk research and ability to understand basics of statistical analysis will be an added advantage. Perks and Benefits PF, Monthly Grocery

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.

You should be an individual with an MSc or MTech degree in Bioinformatics or Computational Chemistry, coupled with 2 to 4 years of experience in the field. Your responsibilities will include being an integral part of a team dedicated to accomplishing project goals successfully, encompassing both industrial and academic projects. It will be your duty to devise innovative project plans for each project under your supervision, and you should demonstrate proactive troubleshooting abilities to handle any experimental challenges that may arise. Your core skills should revolve around expertise in Modelling, Docking, and Molecular Dynamics simulation. Additionally, you should possess a foundational understanding or experience in protein structure, function, dynamics, and engineering. Proficiency in programming and scripting languages such as Fortran, C, C++, Perl, and Python is essential. Strong scientific writing skills are also required, enabling you to produce articles suitable for high-impact factor journals. You should be adept at explaining algorithms and refining them for enhanced outcomes. A collaborative mindset, dedication to team success, and the ability to work autonomously are crucial traits. Exceptional interpersonal and communication skills are highly valued in this role. Moreover, familiarity with tools like Gromacs, Auto dock, and Modeller would be advantageous. If you meet these qualifications and are excited about this opportunity, please send your profiles to Shilpa.ramdurg@quantumzyme.com.,

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.

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.

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols. Should have knowledge in Clinical Data Management EDC Edit Checks SAE Reconcillation Required Candidate profile Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study

Roles and Responsibilities Candidate will be required to do desk research on various domains like English Literature, Social Science and Management and write academic content related to the same. Content in the form of scientific papers, research articles, review papers and literature review will need to be written. Knowledge of systematic literature review, APA citation style, Harvard referencing system would be an added advantage. Desired Candidate Profile An ideal candidate will be a M.A>, M.Sc, MBA, PGDM, Master's in Marketing, Finance, HR, Project Management, Operations Management, or English Literature with excellent English writing skills. Desk research and ability to understand basics of statistical analysis will be an added advantage. Perks and Benefits PF, Monthly Grocery

You have proven experience working in GMP/GLP and scientific environments. You possess basic knowledge of Spectroscopic and Biophysical techniques, Peptide chemistry, as well as peptide characterization. Your expertise lies in at least one of these subjects. Additionally, you have experience in related compound method development and method validation for Peptide drug products using LC-UV and Amino acid analyzer. Hands-on experience with SEC-UV SEC-MALS, SV-AUC, CE, and data interpretation is also one of your strengths in at least one of the techniques and data interpretation. You are skilled in the preparation and review of method development and method validation reports. Knowledge of ICH guidelines and regulatory requirements for peptide products is part of your expertise. As a team player, you are willing to work at different job locations as per the team's requirement. Furthermore, having knowledge of scientific writing will be a plus. Qualifications required for this role include an M. Pharm/M. Sc degree. Amneal is an equal opportunity employer that values diversity and inclusion, ensuring no discrimination based on caste, religion, gender, disability, or any other legally protected status. The Human Resources team at Amneal partners with all aspects of the organization, driving success through effective and innovative people management for both current and future business needs. The team performs key roles such as: - Executive Role: Specialists in all aspects of people management, providing high-level strategic input into key business decisions. - Audit Role: Ensuring compliance with legal requirements and best practice employment policies and procedures across the organization. - Facilitator Role: Partnering closely with different areas of the organization to support, advise, and enhance their ability to meet objectives through highly effective employment practices in areas like Talent Acquisition, Learning and Development, Reward systems, Performance Management, and Health and Wellbeing. - Consultancy Role: Providing expert advice to the organization and its managers on various aspects of workforce management, employee relations, and performance. - Service Role: Keeping the organization informed and equipped to handle developments impacting employment matters, including changes in legislation and labor market characteristics.,

As a Scientist in the Bio-Sciences department at Loyola Centre for Research & Development (Xavier Research Foundation), located in Ahmedabad, Gujarat, India, you will be responsible for conducting research in the field of Bio-Sciences. This is a full-time, mid-level position in the Research & Development, Biotechnology, and Education industry. Your work will primarily involve research, scientific writing, data analysis, and laboratory management. Reporting to the Research Department, you will be expected to have a Doctorate (Ph.D.) in a Bioscience field, with a minimum of 3 years of experience, as evidenced by a requirement of at least 3 publications as the primary author in high impact factor journals. Your key qualifications include expertise in research methodologies, scientific writing, data analysis, and laboratory management. The compensation for this position ranges from 35,000 to 40,000 Indian Rupees per month, depending on your experience and qualifications. This is a permanent, full-time position based at St. Xavier's College Campus in Ahmedabad, Gujarat, India. The work schedule is full-time on-site. To apply for this position, please submit your CV/Resume by email to lcrd@xrf.res.in before the application deadline on August 8, 2025. For any inquiries or to learn more about the application process, you can contact us at 079-26300386.,

correct Job description: If you are interested, please call 9094200201 and email your resume to rajesh_r@jrkresearch.com. Location: Kundrathur, Chennai Job Definition : i. To be responsible for converting scientific and technical product information and studies of medicaments and cosmetic preparations into requirements that suit various use situations for marketing and sales communications to medical practitioners, customers in print, digital and offline modes. ii. To supervise and assist in creative design and ensure accuracy and completeness of such promotional and communication materials within defined timelines and coordinate with relevant internal and external resources. iii. To present the outcomes of the above to sales and marketing teams from time to time. Skill : i. Strong reading, writing and spoken communication skills in English and atleast one or two regional languages ii. Proficiency in Microsoft Office applications including MS PowerPoint, MS Word, MS Excel iii. Analytical skills to interpret technical and outcome data and present in simple forms like Graphs and tables iv. Multi-tasking skill v. Ability to assemble/collate information from multiple sources and simplify/present for the intended purpose/audience vi. Willingness to learn, adapt and adopt. vii. Proofreading /Attention to detail Knowledge /Experience : i. Reasonable familiarity with human physiology, research studies, diseases and disorders, treatment options ii. Prior experience in support activities in pharmaceutical/hospital/ research establishments in related areas including preparation of promotional materials like flyers, brochures, banners etc both print and digital iii. Two to five years of relatable experience. Qualification: Masters in Biotechnology/Pharm-D /MSC Life Sciences.

As a Clinical Microbiologist & Infection Control Officer at HaystackAnalytics, a HealthTech company based in Navi Mumbai, you will be an integral part of our Medical Affairs team. Your role will involve collaborating closely with the Medical Affairs Head to support reporting, documentation, and data analysis for clinical and scientific projects. You will have the opportunity to contribute to the interpretation and presentation of clinical data, coordinate internal communications within the team, and participate in various medical discussions and training sessions. Your responsibilities will include drafting, reviewing, and organizing scientific and clinical reports, maintaining confidentiality and accuracy in handling medical documents and sensitive clinical data, and staying updated on developments in microbiology and infectious disease diagnostics. Additionally, you will be expected to understand the microbiological and clinical aspects of our products and effectively communicate this information in a professional manner. Sharing relevant case studies, clinical experiences, or infection trends to highlight product effectiveness will be a key aspect of your role. We are looking for a Fresher with an MD specialization in Microbiology (Completed) and a strong academic background in infectious diseases, clinical microbiology, and diagnostics. Excellent documentation and communication skills are essential, along with a proactive attitude, high attention to detail, and willingness to travel and participate in in-person meetings as required. Proficiency in Microsoft Office tools and scientific writing is preferred, along with a demonstrated understanding of infection control protocols, antimicrobial stewardship principles, and molecular technologies such as Next-Generation Sequencing (NGS). In this role, you will gain valuable experience in supporting cutting-edge medical research and genomic diagnostics, work with a highly accomplished Medical Affairs team, and have exposure to real-world clinical documentation and healthcare innovation. You will have opportunities for professional growth and learning in a mission-driven healthcare environment, particularly in the field of advanced sequencing technology in the diagnostic industry. Additionally, we offer a competitive salary commensurate with experience and a comprehensive health benefits package. If you are passionate about microbiology, infectious diseases, and diagnostics, and eager to contribute to a dynamic and collaborative team environment, we encourage you to apply for this position and be part of our innovative journey at HaystackAnalytics.,

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols Recruit, screen, and enroll study participants while maintaining accurate documentation and records Required Candidate profile Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study

Clin Infotech is offering the internship opportunity for BDS MDS Dental Graduates Should have Knowledge in Pharmacovigilance Should Have knowledge on Argus & MEDDRA Applicants Should Complete Certification in Pharmacovigilance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage

Perform triage & intake of ICSR received daily in ARGUS databases Should have hands On Experience On ARGUS Safety Database Should Have hands on Experience on MEDDRA Applicants Should Complete Certification in Pharmacoviiglance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage

Medical Writer / Technical Content Writer - Internship This internship is ideal for someone passionate about simplifying medical or technical information into clear, structured documents and engaging content. Good Knowledge of Medical terminology. Required Candidate profile Preparation of protocol for Clinical trials Preparation writing CSR (Clinical Study Report) BDS and MBBS With medical writing for clinical trials Knowledge are Applicable

As a Medical Writer with our dynamic team, you will utilize your expertise in writing, editing, and reviewing scientific and medical content. Your primary responsibility will involve transforming intricate medical data and research findings into clear, accurate, and engaging documents suitable for various audiences, including healthcare professionals, regulatory bodies, and the general public. You will be expected to develop, write, and edit a diverse range of documents such as clinical study reports, regulatory submission documents, peer-reviewed publications, and educational materials. Your role will also involve generating high-quality manuscripts, abstracts, posters, and presentations for scientific conferences, journals, and other platforms. Collaboration is key in this role as you will work closely with researchers, clinicians, regulatory affairs professionals, and other stakeholders to ensure that all content aligns with regulatory standards, maintains scientific accuracy, and supports corporate objectives. Additionally, you will be responsible for preparing and revising documents for regulatory submissions, ensuring compliance with guidelines from regulatory bodies such as FDA, EMA, and ICH. Your tasks will also include conducting literature searches, reviewing existing medical research, and ensuring the accuracy and relevance of information to support content development. Quality assurance is crucial as you will be editing and proofreading content for clarity, consistency, accuracy, grammar, and adherence to style guides. Project management skills are essential as you will be managing timelines for multiple projects to ensure timely and efficient completion of tasks. Compliance with medical, ethical, and regulatory standards is a core requirement for this role. To qualify for this position, you should hold a degree in BAMS, BDS, MBBS, or Pharm D, along with a minimum of 2 years of experience in medical writing, medical coding, or a related field. Experience with regulatory documents is highly preferred. A strong understanding of clinical research, medical terminology, and regulatory guidelines is essential. Proficiency in Microsoft Office Suite, reference management software, and medical writing software is required. Excellent written and verbal communication skills are essential, with the ability to convey complex information clearly and concisely. Strong attention to detail, collaboration skills, and the capability to work independently and as part of a team in a fast-paced environment are also necessary. Exceptional command of the English language is required, and knowledge of additional languages is a plus. Desirable skills for this role include experience with writing for regulatory agencies, familiarity with scientific publishing and journal submission processes, knowledge of Good Clinical Practice (GCP), and experience with statistical analysis and interpretation of clinical data. This is a full-time, permanent position with benefits including provided food, health insurance, and Provident Fund. The work schedule is a day shift with a fixed location in person. The application deadline is 31/07/2025.,

Education - MD specialisation in Microbiology. Job Summary We are seeking a dedicated MD in Microbiology to join our Medical Affairs team. The role involves close collaboration with the Medical Affairs Head to support reporting, documentation, and data analysis related to clinical and scientific projects. The position is based in Navi Mumbai, with potential travel and meeting participation as part of the job. What We Want You To Do Assist the Medical Affairs Head in drafting, reviewing, and organizing scientific and clinical reports. Analyze clinical data and contribute to interpretation and presentation of findings. Coordinate internal communications and documentation flow within the Medical Affairs team. Attend and support internal and external meetings, medical discussions, and training. Liaise with cross-functional teams including Sales, and Operations. Maintain confidentiality and accuracy in handling medical documents and sensitive clinical data. Stay updated on developments in microbiology and infectious disease diagnostics. Understand the microbiological and clinical aspects of our products in a clear and professional manner. Share relevant case studies, clinical experiences, or infection trends to highlight product effectiveness. Maintain a strong understanding of emerging microbiological trends and technologies, including Next-Generation Sequencing (NGS). Optionally participate in Continuing Medical Education (CME) programs and Round Table Meetings (RTMs) What Are We Looking In You Fresher - MD in Microbiology (Completed). No other educational qualifications will be considered. Strong academic foundation in infectious diseases, clinical microbiology, and diagnostics. Excellent documentation and communication skills. Eagerness to work in a collaborative environment with dynamic responsibilities. Willingness to travel and participate in in-person meetings as required. High attention to detail, time management, and a proactive attitude. Proficient in Microsoft Office tools and scientific writing (preferred). Demonstrated understanding of infection control protocols and antimicrobial stewardship principles. Familiarity with molecular and sequencing (NGS) technologies and their applications in clinical microbiology is advantageous. Open to travel to PAN India for CME programs and RTMs. What You Will Gain Experience in supporting cutting-edge medical research and genomic diagnostics. Opportunity to work with a highly accomplished Medical Affairs team. Exposure to real-world clinical documentation and healthcare innovation. Professional growth and learning opportunities in a mission-driven healthcare environment. Experience in working with advanced sequencing technology in the diagnostic industry i.e. NGS, WGS, Nanopore, and Illumina. Competitive salary commensurate with experience Comprehensive health benefits package

Scientific Lead - Medical Nutrition (MD) Are you a medical doctor with deep clinical expertise, a flair for scientific storytelling, and strong KOL relationships in Delhi NCR? What You will Do: Act as the scientific face of the organization for clinical nutrition solutions Engage meaningfully with key medical experts across critical care, internal medicine, respiratory medicine, and nutrition therapy Drive scientific education, knowledge sharing, and real-world clinical insights across the medical community Collaborate closely with commercial, marketing, and regulatory teams to align strategy and communication Lead initiatives to develop regionally relevant clinical evidence. What Were Looking For: MD in Internal Medicine, Pulmonary Medicine, Critical Care, Pharmacology, or Biochemistry 8 to10 years of experience in medical affairs or scientific roles within pharma, biotech, or medical nutrition domains Strong connections with KOLs in Delhi NCR across relevant specialties (must-have) Excellent command over scientific communication (written + presentation) Sound understanding of compliance, clinical evidence, and regulatory nuances. Why This Role: Lead the scientific voice behind an innovative product launch in the Indian medical nutrition space Operate in a lean setup with strong global backing Influence real outcomes for patients dealing with complex nutritional challenges Location: Gurugram (frequent travel across key metro cities) If youre ready to lead from the front and shape the clinical positioning of next-gen nutrition products, send your CV and a short note highlighting your MD specialization and KOL experience in Critical Care / Nephrology / Respiratory / Oncology etc.