Job DescriptionWe are a research:driven biopharmaceutical company. Our mission is built on the simple premise that if we "follow the science" and that great medicines can make a significant impact to our world. And we believe that a research:driven enterprise dedicated to world:class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, MSD policies and procedures, quality standards and adverse event reporting requirements internally and externally.Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expand the territory for clinical research, finding and developing new sites. Participates in internal meetings and workstreams as SME for monitoring processes and systems.Responsibilities include, but are not limited to:Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.Performs clinical study site management/monitoring activities in compliance with ICH:GCP, Sponsor SOPs, Local Laws and Regulations, Protocol, Site Monitoring Plan and associated documents.Gains an in:depth understanding of the study protocol and related procedures.Coordinates and manages various tasks in collaboration with other sponsor roles to achieve Site Ready. - Participates and provides inputs onsite selection and validation activities.Performs remote and on:site monitoring and oversight activities using various tools to ensure:- Data generated at site are complete, accurate and unbiasedSubjects' right, safety and well:being are protectedConducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close:out visits and records clear, comprehensive and accurate visit and non:visit contact reports appropriately in a timely manner.Collects, reviews, and monitors required regulatory documentation for study start:up, study maintenance and study close:outmunicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.Identifies, assesses and resolves site performance, quality or compliance problems and escalates per defined CRA Escalation Pathway as appropriate in collaboration with CRA manager, CRM, and RCPM. - Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor and sharing best practices as appropriate/required.Supports and/or leads audit/inspection activities as neededFollowing the country strategy defined by CRD and CRA manager, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilitiesCORE Competency Expectations:Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively.Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH and country clinical research law and guidelines.Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines. - Hands on knowledge of Good Documentation Pract
