OverviewCOSS-0, Associate Director, SSUL, Clinical Site Agreements – Merck HealthcareJoin to apply for the COSS-0, Associate Director, SSUL, Clinical Site Agreements role at Merck Healthcare.Work Your Magic with us! Ready to explore, break barriers, and discover more? Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.ResponsibilitiesDrive with internal and external business partners in developing the CSA Strategy Plan at study levelServe as CSA delivery expert for high priority studies and oversee the CSA delivery performance at study levelServe as the point of escalation to CSA team members and study teams on clinical site budget and agreement process issues and facilitate resolution to the issuesEnsure globally approved CSA templates are utilized at study level and coordinate the revisions of Master Clinical Site Agreement/Master Confidentiality Agreement templates and Legal ManualsLead, develop and update negotiating parameter guidance documents (which include agreed grant plan budget limit, contract language, apply forward terms and fixed item cost sheets) with internal and external business partners at Country and Site level (as needed) independentlyApprove Fair Market Value (FMV) assessments for any complexity investigator grant evaluation across the portfolio independentlyManage or approve high level estimates or budget build for any complexity local regional CSS, CRS and global development trials at study, country or site levelPerform Confidentiality Agreement customization across the portfolio and lead discussion with Legal where required; coordinate and lead Confidentiality Agreement escalation, evaluation and feedback across the portfolioQualificationsAt least 10 years in clinical research in a CRO or Pharmaceutical/Biotechnology Industry environmentUnderstanding of the overall clinical development paradigm, especially in the area of clinical study operationsAt least 5 years of experience in contract and budget negotiation at Global or Regional level (at least)Experience in oversight of external service providers, preferredExperience in the management of contracts related to additional HCP activities (e.g. SMC, IDMC,...), preferredThorough knowledge of ICH-GCP and applicable laws and regulations for key countriesWhat we offerWe are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!Job detailsSeniority level: Mid-Senior levelEmployment type: Full-timeJob function: Research and ScienceIndustries: Pharmaceutical Manufacturing #J-18808-Ljbffr