Senior Medical Writer(scientific Writer & Quality Check)

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Syneos Health
Senior Medical Writer(scientific Writer & Quality Check) (Pune)
Syneos Health · Pune, Maharashtra · via Shine
3 days ago
Full–time
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Job description
Updated Yesterday Location Pune MH India Job ID hidden_mobile3 Description Senior Medical Writer Scientific writer Quality check Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical medical affairs and commercial insights into outcomes to address modern market realities Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with but to make us easier to work for Whether you join us in a Functional Service Provider partnership or a Full-Service environment youa ll collaborate with passionate problem solvers innovating as a team to help our customers achieve their goals We are agile and driven to accelerate the delivery of therapies because we are passionate to change lives Discover what our 29 000 employees across 110 countries already know WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people through career development and progression supportive and engaged line management technical and therapeutic area training peer recognition and total rewards program We are committed to our Total Self culture a where you can authentically be yourself Our Total Self culture is what unites us globally and we are dedicated to taking care of our people We are continuously building the company we all want to work for and our customers want to work with Why Because when we bring together diversity of thoughts backgrounds cultures and perspectives a wea re able to create a place where everyone feels like they belong Job Responsibilities JOB SUMMARY Serves as a senior medical writer on clinical study or regulatory or publication project teams Writes edits and coordinates content for clinical regulatory scientific while serving as primary technical contact with the internal team and the client JOB RESPONSIBILITIES Mentors and leads less experienced medical writers on complex projects as necessary Acts as lead for assigned writing projects Manages medical writing activities associated with individual studies coordinating medical writing activities within and across departments with minimal supervision Develops or supports a variety of documents that include but not limited to Clinical journal manuscripts clinical journal abstracts posters and oral presentations Identifies and proposes solutions to resolve issues and questions arising during the writing process including resolution or escalation as appropriate Reviews statistical analysis plans and table figure listing specifications for appropriate content and for grammar format and consistency Interacts with department head and staff members in data management biostatistics regulatory affairs and medical affairs as necessary to produce writing deliverables Serves as peer reviewer on internal review team providing review comments on draft and final documents Adheres to established regulatory standards including but not limited to Journal congress specific guidelines as well as Company Standard Operating Procedures client standards and Company and or client approved templates when completing medical writing projects on-time and on-budget Performs on-line clinical literature searches as applicable Familiarity with figure-creation and data visualization software including tools such as GraphPad Prism and Adobe Illustrator for developing high-quality scientific figures and graphics Familiarity with publication planning software e g Datavision and PubConnect VeevaVault Promomats Reviews deliverables for scientific accuracy data and referencing quality appropriate style and correct branding of scientific medical assets Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing Maintains awareness of budget specifications for assigned projects working within the budgeted hours and communicating changes to medical writing leadership Completes required administrated tasks within the specified timeframes Performs other work-related duties as assigned Minimal travel may be required less than 25 QUALIFICATION REQUIREMENTS Bachelor of Science degree with relevant writing experience or Bachelor of Arts degree Social Sciences English or Communications preferred with relevant scientific and or medical knowledge and expertise Extensive knowledge of English grammar and FDA and ICH regulations and guidelines as well as a familiarity with AMA style guide Demonstrated high degree of independence with effective presentation proofreading interpersonal and leadership skills and ensure a team-oriented approach Strong proficiency in Word Excel PowerPoint email and Internet Ability to demonstrate a familiarity with principles of clinical research and to interpret and present clinical data and other complex information Get to know Syneos Health Up