Job Description:Here at Syneos Health we are currently recruiting for a Medical Affairs Scientist Why Syneos Health #SyneosHealthLife means were committed to our Total Self culture where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every persons unique contributions make a difference. We believe our success is a direct result of the people who are driving it you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you. Thats why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial.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 were able to create a place where everyone feels like they belong. Job details:The Medical Scientist will partner with one or more Medical Directors to provide scientific input to clinical development programs, with an emphasis on ensuring scientific integrity of clinical trial data. The Medical Scientist will collaborate with Medical Directors and cross-functional team members on data reviews and may support other Medical Management activities for successful execution and conduct of clinical trials. Responsibilities for this role are as follows:Conducts regular and ad-hoc review of clinical data to identify risks and data patterns or trends under the supervision of the Medical Director(s), using one or more of the following tools:Kick-Off Meetings, Investigator Meetings, and Medical Meetings. Collaborates with Medical Director(s) and Functional Lead(s) to manage activities related to Medical Committees, if in scope (e.G., Safety Review Committees Steering Committee meetings,etcetera). OTHER RESPONSIBILITIES:MSc Degree in life sciences, RN, PharmD, PhD, MD, or equivalent with relevant scientific experience and/or training discipline Must possess an understanding of scientific principles to assure effective and high quality scientific and medical data review Must have excellent time management techniques to handle multiple tasks and deadlines while delivering high quality work in a highly regulated and dynamic environment Must have ability to adapt to fluctuating timelines, work demands and changes in scope of work Ability to troubleshoot situations and demonstrate judgment to invoke leadership support when needed Must possess excellent written and oral communication skills,to include compilation and delivery of presentations to internal and external stakeholders Must demonstrate excellent technology skills including MS Office programs, spreadsheets, presentation tools, and use of databases Prior knowledge of drug development and demonstrated proficiency with ICH/GCP guidelines preferred Strong team player with excellent interpersonal skills and ability to work effective in a cross-functional team environment #J-18808-Ljbffr