518 Scientific Writing Jobs - Page 14

We are seeking highly motivated individuals with a strong foundation in academic and scientific writing. The ideal candidate should have a solid understanding of research methodology, literature reviews, referencing styles, and publication standards. Familiarity with data analysis tools and research survey techniques will be highly valued Key Responsibilities: Create and refine academic and scientific content across disciplines Conduct thorough literature reviews and identify research gaps Develop content for research papers, review articles, surveys, and book chapters Write structured methodology and result interpretation sections Maintain accurate referencing using styles such as APA, IEEE...

Role & responsibilities: Main experience in CSR safety narratives writing (authoring, addressing review comments, collaborating with teams) Compiles, writes, edits, and coordinates medical writing deliverables that present scientific information clearly and accurately, and works as a medical writer within and across departments with minimal or moderate supervision. • Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports; journal manuscripts; and abstracts, po...

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, social media posts, websites, digital and print brochures, banners, and more. You will be responsible for ensuring that the content for Novartis Brand/products reflects the most recent changes to Important Safety Information (ISI), Prescribing Information (PI), and other reference documents. It is crucial that these updates adhere to the stringent MLR guidelines and specifications (Medical-Legal-Regulatory). As part of the "Creative" team under Centralized Asset Support Team (CAST), you will collaborate close...

As an Intern in CMC (Formulation) at Ferring India FHPDC R&D, you will be part of the CMC (Formulation) department in Hyderabad for a duration of 12 months. Reporting to the Lead Scientist - CMC (Formulation), you will receive a stipend for your work. To qualify for this position, you should have a Masters degree in Pharmaceutical Sciences (Pharmaceutics) or a related discipline from a reputable institution. A strong academic background in pharmaceutics is essential, along with basic knowledge of formulation principles and analytical techniques. Familiarity with regulatory guidelines such as ICH, FDA, and EMA is advantageous. Proficiency in MS Office (Word, Excel, PowerPoint) and scientific ...

The candidate should be a MSc or MTech (Bioinformatics/Computational Chemistry) graduate with 2-4 years of experience. The annual salary will be as per market standard and the location of the job is Bengaluru. As a member of the team, you will play a key role in achieving project goals for both industrial and academic projects. You will be responsible for developing creative project plans and proactively troubleshooting any problems that may arise during experiments. Core skills required for this position include knowledge and experience in Modelling, Docking, and Molecular Dynamics simulation. Additionally, you should have a basic understanding of protein structure, function, dynamics, and ...

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,...

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. ...

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 d...

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 ...

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 Su...

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 ...

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...

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 statist...

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 ...

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 ...

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 guidelin...

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 in...

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 basic...

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 ...

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 fact...

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...

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 confidentiali...

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