Safety & PV Submission Specialist II (Gurugram/Hyderabad)

Requirements

• Bachelor's Degree in life science, 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.
• Experience in a clinical research organization preferred with a minimum of 4 years' Safety and Pharmacovigilance experience required including safety submissions
• Experience in Safety Submissions to regulatoty authorities (Ideal) sites and Ethics committee
• Experience in leading projects for safety submissions work
• TMF Filing and oversight
• Thorough knowledge on PV guidelines, EMEA,FDA and India guidelines
• Ability to work independently and in a team environment
• Strong communication, presentation, interpersonal skills, both written and spoken
• Strong organizational skills with proven ability to prioritize and work on multipl

Benefits

Additional Information

Safety & PV Submission Specialist II (Gurugram/Hyderabad) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: 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 building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life. - We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities Collaborate with the Sponsor and internal project management associates on the design, preparation and assembly of the expedited and periodic safety report documents Participates in project launch activities for safety reporting tasks Prepares Safety Reporting Plan for safety submissions only projects Maintain tracking of safety submissions Provides Sponsor/Customer with expedited and periodic safety report submission status updates, as required Provides support and advice on expedited and periodic safety report issues to project team/Sponsor as required Apply safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities File documents according to project specific requirements (electronically or in hard copy as applicable). Forward completed safety submission documents to clients and other relevant parties Acts as a point of contact for regulatory issues related to safety submissions May be responsible for distributing and monitoring team workload Fosters constructive and professional working relationships with all project team members, internal and external Assists in the preparation and participates in internal project review meetings as required Assists in the tracking and measuring of program/project and team progress through collection of cycle time metrics and other key performance indicators (KPIs), related to submissions. Participates in audits as required/appropriate 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 Maintains an understanding and compliance with Standard Operating Procedures (SOPs), Work Instructions (WIs), global drug/biologic/device regulations, GCPs, ICH guidelines, and the drug development process.

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