Senior Medical Writer
4 days ago
Senior Medical Writer ICON plc is a world-leading healthcare intelligence and clinical research organization We re proud to foster an inclusive environment driving innovation and excellence and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Medical Writer to join our diverse and dynamic team As a Senior Medical Writer at ICON you will play a pivotal role in leading the development and execution of medical writing strategies for clinical trial projects contributing to the advancement of innovative treatments and therapies What you will be doing Leading the preparation review and editing of clinical study documents including clinical study protocols clinical study reports CSRs investigator brochures IBs patient narratives and regulatory submissions CTD modules ensuring accuracy clarity and compliance with regulatory guidelines and industry standards Collaborating closely with cross-functional teams including biostatistics and programming regulatory affairs and medical affairs to interpret and analyze clinical trial data summarize scientific findings and communicate key insights in written form Participating in the planning and execution of clinical development programs providing strategic input and scientific expertise to support the design conduct and interpretation of clinical studies and research initiatives Mentoring and coaching junior medical writers providing guidance on best practices writing techniques and scientific principles and fostering a culture of excellence collaboration and continuous learning within the medical writing team Your profile Advanced degree in Life Sciences Pharmacy Medicine or related field with a minimum of 7 years of experience in authoring of above-mentioned documents in medical writing within the pharmaceutical biotechnology or contract research organization CRO industry Proficiency in interpreting and summarizing complex clinical trial data scientific research findings and statistical analyses with excellent writing editing and proofreading skills and the ability to communicate scientific concepts to diverse audiences Strong understanding of regulatory requirements e g ICH-GCP FDA EMA governing the preparation and submission of clinical documents and publications and experience in interacting with regulatory agencies during the review and approval process Demonstrated ability to work effectively in a fast-paced deadline-driven environment managing multiple projects simultaneously and prioritizing tasks based on project timelines and deliverables Excellent interpersonal and communication skills with the ability to collaborate effectively with cross-functional teams build relationships with key stakeholders and influence decision-making processes What ICON can offer you Our success depends on the quality of our people That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent In addition to your competitive salary ICON offers a range of additional benefits Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family Our benefits examples include Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead Global Employee Assistance Programme TELUS Health offering 24-hour access to a global network of over 80 000 independent specialised professionals who are there to support you and your family s well-being Life assurance Flexible country-specific optional benefits including childcare vouchers bike purchase schemes discounted gym memberships subsidised travel passes health assessments among others Visit our to read more about the benefits ICON offers At ICON inclusion belonging are fundamental to our culture and values We re dedicated to providing an inclusive and accessible environment for all candidates ICON is committed to providing a workplace free of discrimination and harassment All qualified applicants will receive equal consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability or protected veteran status If because of a medical condition or disability you need a reasonable accommodation for any part of the application process or in order to perform the essential functions of a position please let us know or submit a request Interested in the role but unsure if you meet all of the requirements We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles Are you a current ICON Employee Please click to apply
-
Associate Medical Writer
2 days ago
bangalore, India SciVoc™ Consulting Inc. Full timeRole OverviewWe are on the hunt for an Associate Medical Writer eager to turn science into narrative gold. If you’re fascinated by the challenge of translating data into compelling stories and want to learn from leaders in medical communications, this could be your next adventure.As an Associate Medical Writer, you will:Support the senior members with the...
-
Medical Writer
2 weeks ago
Bangalore, India Trigent Software - Professional Services Full timePosition: Senior Medical Writer – RWE Location: Bangalore Job Type: Full-time Department: Medical Writing – MCAPL Job Description The Senior Medical Writer – RWE will be responsible for authoring, reviewing, and managing high-quality scientific and regulatory documents. The role requires strong scientific understanding, writing expertise, and the...
-
Medical Writer
2 weeks ago
bangalore, India Trigent Software - Professional Services Full timePosition: Senior Medical Writer – RWE Location: Bangalore Job Type: Full-time Department: Medical Writing – MCAPL Job Description The Senior Medical Writer – RWE will be responsible for authoring, reviewing, and managing high-quality scientific and regulatory documents. The role requires strong scientific understanding, writing expertise, and the...
-
Medical Writer
1 week ago
bangalore, India Kelly Science, Engineering, Technology & Telecom Full timeJob Title: Medical Writer – Fixed Term Contract (12 months, Full Time) Locations: India, Mexico, Brazil Department: Scientific OperationsAbout the Role: We are seeking a Medical Writer to join a dynamic scientific operations team supporting medical device projects. This is a full-time, site-based role on a 12-month fixed-term contract with the potential...
-
Medical Writer
2 weeks ago
Bengaluru, Karnataka, India ChanRe Healthcare & Research Full timeLifescience/Medical graduate to work as a Medical writer Demonstrated skills in Literature search, Content development Hands on experience with MS office tools, proof reading, Medical thesis writing, Systematic review writing, Meta analysis writing **Salary**: ₹15,000.00 - ₹25,000.00 per month Schedule: - Day shift
-
Senior Content Writer
2 weeks ago
bangalore, India Credex Healthcare Full timeMedical Senior Content Writer (Credentialing & RCM) (Night Shift - Remote) - Work from Home Our client is looking for a senior medical content writer for their US Medical Credentialing & RCM business Domain working 100% Remote in US hours, 9am EST - 6pm EST. This is a full time role working 40 hours/week starting ASAP. We’re looking for someone who can: -...
-
Medical Writer
1 week ago
Mysuru, Karnataka, India Spectrum Talent Management Full time**Job Title: Medical Writer** **Key Responsibilities**: - **Medical Writing**: Create, review, and edit high-quality, scientifically accurate documents including Clinical Evaluation Reports (CERs), Post-Market Surveillance (PMS) reports, and Periodic Safety Update Reports (PSURs). - **Regulatory Compliance**: Ensure that all documents meet regulatory...
-
Medical Writer
2 weeks ago
bangalore, India PDC CRO Full timePharmaceutical Development Company is a leading clinical research organization, providing a Full-Service End-to-End Solution for Phase I to IV clinical trials and NIS /RWE studies in the Middle East and Africa region. Our clients include pharmaceutical, biotechnology, medical device industries, other CROs, and academic organizations. Our team is experienced...
-
Medical Specialist
1 week ago
bangalore, India Second Medical Opinion (SMO) Full time🌟 We Are Hiring Senior Medical Specialists Across IndiaSecond Medical Online Opinion (SMO) – Transforming Patient Care NationwideSecond Medical Online Opinion (SMO) is building India’s most trusted network of senior medical specialists to offer ethical, unbiased, evidence-based second opinions to patients across the country.We are expanding rapidly...
-
Junior Medical Writer
3 days ago
Bengaluru, Karnataka, India Healthminds Consulting Full time**Position: Junior Medical Writer**: **Education qualification**: Masters in Life Science/Dental/Pharma and has knowledge of publications **Experience**: 1 year minimum in content development highly desired **Skills**: - Ability to summarize content from published literature in a concise and meaningful manner, relevant to objectives provided by client. -...