SAS I (Due Diligence Specialist) assigned to client Home Based Mexico Updated: YesterdayLocation: Tlalnepantla, MEX, MexicoJob ID: Description 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. We support a diverse, equitable and inclusive culture and are committed to the Americans with Disabilities Act, including the provision of reasonable accommodations. Why Syneos Health We are passionate about developing our people through career development, supportive line management, technical training, peer recognition and a total rewards program. We uphold our Total Self culture – where you can authentically be yourself. We build a company where diversity of thoughts, backgrounds, cultures and perspectives creates a place where everyone feels they belong. Job Responsibilities Perform assigned activities that lead to startup of investigative sites in all phases of clinical trials, including investigator site contracts, ethics and regulatory submissions, and review of essential documents for site initiation and activation. Ensure local activities follow agreed timelines, budgets and quality standards, and track milestone progress in the SSU tracking system. Act as the main contact with Regulatory Authorities (RA) and Central/Regional Ethics Committees (ECs) under supervision; directly interact with customers regarding RA requirements. Monitor basic financial aspects of the project and hours/tasks available per contract; address discrepancies in a timely manner. Review and comply with SOPs and Work Instructions; keep training records and timesheet compliance up to date. Submit to the Trial Master File (TMF) as per company SOP/Sponsor requirements. Perform functions at the country level, including: Local Submissions Specialist – compile and review essential document packages for site activation. Prepare and submit EC/RA applications and ongoing notifications. Act as liaison between investigational sites and functional leads. Support site selection and feasibility as part of the PM/SAM team. Assist in site contract and budget negotiation as needed. Qualifications Associate’s Degree or equivalent education and training. Good understanding of clinical trial process across Phases II-IV and ICH GCP; ability to interact effectively with investigative site personnel. Good organizational skills, attention to detail, and ability to handle multiple tasks independently. Ability to take direction from multiple individuals and set priorities accordingly. Strong communication skills across multiple function groups (clinical team, PM, Director). Problem‑solving skills and ability to work independently or as part of a team. Quality‑driven approach to all managed activities. Flexibility and willingness to adapt quickly to changing environments and learn new functions. Strong computer skills – Word, Excel, PowerPoint, Publisher. Equal Employment Opportunity This posting complies with all equal opportunity laws and the Americans with Disabilities Act. #J-18808-Ljbffr