[30/10/2025] Sr Safety Specialist

Updated Yesterday Location Gurgaon HR India Job ID 25102421 Description Sr Safety Specialist Literature Review 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 a Conduct systematic and ad-hoc literature searches in global biomedical databases e g Embase PubMed Medline for ICSR identification and safety-relevant information a Skilled in extracting and summarizing key safety information from identified literature sources a Thorough understanding of creating and validating search strategies for pharmacovigilance purpose a In depth knowledge of major literature databases such as Embase PubMed etc a Experience in conducting local literature searches and reviews a Understanding of regulatory requirements with respect to global and local literature a Coordinating workflow to ensure delivery of project a Prepares Safety Management Plan a Assists in the preparation and participates in internal project review meetings as required a May enter information into PVG quality and tracking systems for receipt and tracking ICSR a May process ICSRs according to Standard Operating Procedures SOPs and project program- specific safety plans o Triages ICSRs evaluates ICSR data for completeness accuracy and regulatory report ability o Enters data into safety database o Codes events medical history concomitant medications and tests o Compiles complete narrative summaries o Assesses information to be queried and follows up until information is obtained and queries are satisfactorily resolved o Participates in the generation of timely consistent and accurate reporting of expedited reports in accordance with applicable regulatory requirements o Coordinates with data management staff concerning reconciliation of safety data between the clinical and safety databases a Ensures distribution of all required individual expedited and periodic reports for both clinical and post-marketing projects to the Safety Submissions team if contracted to submit the reports a Provides training of Investigators on ICSR reporting a Participate in audits inspections as required a Ensures all relevant documents are submitted to the Trial Master File TMF as per company SOP Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate a Maintains understanding and compliance with SOPs Work Instructions WIs global drug biologic device regulations GCPs ICH guidelines GVP project program plans and the drug development process What wea re looking for a Bachelora s Degree Postgraduate in health profession with relevant experience registered nurse pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge skills and abilities to perform the job a Minimum 5 years of relevant experience in Pharmacovigilance Literature case reviewing Global Local Identifying NICR Signal AR report from Literature a Strong exposure to quality checks citation reviews and leading internal meetings a Experience in mentoring training work allocation workflow management and QC function oversight a Strong communication skills and solid understanding of medical terminologies and literature review process a Safety Database systems and knowledge of medical terminology required a In depth understanding of clinical trial process across Phases II-IV and or post-marketing safety requirements ICH GCP GVP and regulations related to Safety and Pharmacovigilance a Proficiency in Microsoft Office Suite Word Excel and PowerPoint Visio email Outlook TeamShare or other management shared content workspace and internet a Ability to work independently and in a team environment a Strong organizational skills with proven ability to prioritize and work on multiple tasks and projects a Detail oriented with a high degree of accuracy and ability to meet deadlines a Able to make effective decisions a Minimal travel may be required up to 10 Get to know Syneos Health Over the past 5 years we have worked with 94 of all Novel FDA Approved Drugs 95 of EMA Authorized Products and over 200 Studies across 73 000 Sites and 675 000 Trial patients No matter what your role is youa ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment Learn more about Syneos Health Additional Information Tasks duties and responsibilities as listed in this job description are not exhaustive The Company at its sole discretion and with no prior notice may assign other tasks duties and job responsibilities Equivalent experience skills and or education will also be considered so qualifications of incumbents may differ from those listed in the The Company at its sole discretion will determine what constitutes as equivalent to the qualifications described above Further nothing contained herein should be construed to create an employment contract Occasionally required skills experiences for jobs are expressed in brief terms Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates including the implementation of the EU Equality Directive in relation to the recruitment and employment of its employees The Company is committed to compliance with the Americans with Disabilities Act including the provision of reasonable accommodations when appropriate to assist employees or applicants to perform the 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