{"id":2795794,"url":"https://alion.io/job/parexel-site-care-partner","title":"Site Care Partner","company":{"id":2735,"name":"Parexel","domain":"parexel.com","url":"https://alion.io/company/parexel","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":80,"open_postings":39,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":10,"computed_at":"2026-10-20T05:45:00Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":"staff","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Mumbai, India"],"countries":["IN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":17500,"max_usd":43000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":263},"experience_years_min":10,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false}],"status":"live","first_seen_at":"2026-07-31T00:00:00Z","employer_posted_date":"2026-07-31","last_verified_at":"2026-10-19T22:40:55Z","board_verified":true,"closed_at":null,"days_open":81,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":81},"description":"When our values align, there's no limit to what we can achieve.\nAt 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.\nEach 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.\nAbout Parexel\nParexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.\nWe work with focus, agility, and shared purpose - moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart.\nAbout the Role\nWe are seeking a Site Care Partner to join our team in a Hybrid (Mumbai) capacity. As a Site Care Partner, you will support clinical research activities that advance new treatments for patients. This position plays a key role in study execution, patient safety oversight, regulatory compliance, and clinical data accuracy. You'll collaborate with cross-functional teams, follow industry-standard processes, and contribute to study operations from planning through closeout.\nResponsibilities include providing essential support to clinical research sites, managing study documentation, ensuring regulatory compliance, and maintaining the highest standards of patient care and data integrity. With diverse teams and continuous learning opportunities, the Site Care Partner can explore career paths and expand skills across clinical research.\nKey Responsibilities\nSupport site initiation, monitoring, and closeout activities to ensure compliance with protocol requirements and regulatory standards.\n\nMaintain and organize study documentation, including regulatory files, correspondence, and study records.\n\nAssist with patient recruitment, enrollment, and informed consent processes while maintaining ethical standards.\n\nSupport data collection and verification activities to ensure accuracy and completeness of clinical trial data.\n\nCoordinate with site personnel, sponsors, and internal teams to address study-related issues and maintain effective communication.\n\nMonitor adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements throughout the study lifecycle.\n\nPrepare reports and documentation required for regulatory submissions and study audits.\n\nContribute to continuous improvement initiatives and share best practices across the clinical research team.\n\nYou'll thrive in this role if you bring\nStrengths in organization, communication, and attention to detail.\n\nExperience working in clinical research, healthcare, or a regulated environment.\n\nThe ability to collaborate across teams and communicate clearly with diverse stakeholders.\n\nA patient-focused mindset and commitment to maintaining the highest standards of data integrity.\n\nComfort working with clinical trial management systems and electronic documentation platforms.\n\nRequired Qualifications\nDemonstrated experience in site management with prior experience as a Clinical Research Associate (CRA).\n\nHigh school diploma or equivalent.\n\n10+ years of experience in clinical research, study operations, healthcare, or a related field.\n\nKnowledge of ICH-GCP, regulatory requirements, and clinical trial processes.\n\nExperience with clinical trial 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