Senior Clinical Research Associate

When our values align, there's no limit to what we can achieve. At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. PXL FSP has an exciting opportunity for a Senior CRA ! The Senior Clinical Research Associate is responsible for the following: Act as the primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Key Accountabilities: Site Management Responsibilities 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 & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the study protocol and related procedures. Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready. Participates & provides inputs on site selection and validation activities. Performs remote and on-site monitoring & oversight activities using various tools to ensure: Data generated at site are complete, accurate and unbiased. Subjects’ right, safety and well-being are protected. Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & 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-out. Communicates 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, TA Head and CRD as needed. Works in partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites. Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines. Team Development and Support Contributes strongly to CRA team knowledge by acting as process Subject Matter Expert (SME), sharing best practices, making recommendations for continuous improvement and providing training as appropriate/required. Supports and/or leads audit/inspection activities as needed. Mentors / buddies junior CRAs on process/study requirements and performs co-monitoring visits where appropriate. Contributes to initiatives and projects adding value to the business Performs co-monitoring as appropriate Compliance with Parexel Standards • Comply with required training curriculum • Complete timesheets accurately as required • Submit expense reports as required • Update CV as required • Maintain a working knowledge of and complies with Parexel /Client processes, ICH-GCPs and other applicable requirements Skills: • Fluent in local languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively • Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP / ICH and country clinical research law and guidelines • Hands on knowledge of Good Documentation Practices • Excellent understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines • Demonstrated ability to mentor/lead • Proven skills in Site Management including independent management of site performance and patient recruitment • Demonstrated high level of monitoring skill with independent professional judgement • Good IT skills (Use of MS office, use of various clinical IT applications on computer