{"id":3088849,"url":"https://alion.io/job/merck-co-clinical-research-associate-5","title":"Clinical Research Associate","company":{"id":3768,"name":"Merck & Co.","domain":"msd.com","url":"https://alion.io/company/msd","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":99,"open_postings":118,"ghost_share":0.008,"stale_share":0.136,"repost_share":0.127,"time_to_fill_p50_days":15,"computed_at":"2026-10-28T05:59:10Z"}},"role":"Biotech","role_family":"Biotech","seniority":null,"employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"posting_text","remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["London, United Kingdom"],"countries":["GB"],"hiring_countries":["GB"],"hiring_countries_total":1,"salary":null,"salary_estimate":{"min_usd":68000,"max_usd":145000,"period":"year","method":"role_country_seniority_unknown","sample_n":19},"experience_years_min":null,"visa_sponsorship":true,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Good Clinical Practice","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-10-22T14:19:30Z","employer_posted_date":"2026-10-22","last_verified_at":"2026-10-29T02:35:46Z","board_verified":true,"closed_at":null,"days_open":6,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":6},"description":"Job Description\nClinical Research Associate\nLocation: UK Nationwide\nTravel: Approximately 65-75% (about 2-3 days per week, domestic and international)\nAbout our company Our company is committed to advancing high-quality clinical research that upholds ICH/GCP standards and local regulatory requirements. We collaborate across global and regional teams to deliver studies with excellence, integrity, and patient safety at the core.\nRole overview We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within the South East. Under the oversight of the CRA Manager or Clinical Research Director (CRD), you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local regulations, our company policies and procedures, quality standards, and adverse event reporting requirements.\nYou will take ownership of allocated sites, actively expand our clinical research territory by identifying and developing new sites and contribute as a subject matter expert on monitoring processes and systems across internal workstreams.\nKey responsibilities\nBuild and sustain strong relationships with investigative sites across all trial phases.\nPerform site management and monitoring activities in compliance with ICH-GCP, Sponsor SOPs, local laws/regulations, protocol, site monitoring plans, and related documents.\nDevelop deep understanding of study protocols and procedures.\nCoordinate cross-functional tasks to achieve Site Ready status.\nParticipate in site selection and validation; provide informed input to decisions.\nConduct remote and on-site monitoring to ensure:Data integrity (complete, accurate, unbiased).\nProtection of subjects’ rights, safety, and well-being.\n\nExecute validation, initiation, monitoring, and close-out visits; document clear, comprehensive visit and non-visit reports in a timely manner.\nCollect, review, and monitor regulatory documentation for start-up, maintenance, and close-out.\nCommunicate proactively with investigators and site staff on protocol conduct, recruitment/retention, deviations, regulatory findings, audits/inspections, and site performance.\nIdentify, assess, and resolve site performance, quality, or compliance issues; escalate appropriately per the CRA escalation pathway in collaboration with CRA Manager, CRM, TA Head, and CRD.\nPartner with internal teams (country operations, finance, regulatory affairs, pharmacovigilance, legal, regional operations, HQ) and external stakeholders (vendors, IRB/IEC, regulatory authorities).\nMaintain accurate, timely documentation in CTMS, eTMF, and other systems.\nAct as a process SME: share best practices, drive continuous improvement, and deliver training.\nSupport and/or lead audit/inspection activities.\nContribute to country strategy by identifying and onboarding potential new sites; build site capabilities.\nMentor and buddy junior CRAs; conduct co-monitoring and quality control visits where appropriate.\nTravel requirements\nAbility to travel domestically and internationally approximately 65-75% of working time (about 2-3 days per week).\nValid driver’s license preferred; required in certain countries.\nQualifications, skills, and experience\nCore competencies\nFluent in English, with strong written and verbal communication skills and the ability to present technical information effectively.\nRobust knowledge of clinical research, trial phases, ICH/GCP, and local clinical research regulations and guidelines; ability to work within global, country, and regional frameworks.\nDemonstrated mentoring and leadership capability.\nHands-on knowledge of Good Documentation Practices.\nProven site management expertise, including independent oversight of site performance and patient recruitment.\nHigh-level monitoring skills with sound, independent professional judgment.\nStrong IT proficiency (MS Office and clinical applications across computer, tablet, and mobile); adaptable to new tools.\nAbility to interpret data/metrics and take appropriate action, including in virtual settings.\nExperience conducting site motivation visits to boost enrollment.\nSolution-oriented approach to complex issues; capable of root cause analysis and implementing preventive/corrective actions.\nAbility to mentor junior CRAs and perform co-monitoring visits.\nBehavioral competencies\nExcellent time management, organization, interpersonal skills, conflict management, and problem solving.\nHigh independence across multiple protocols, sites, and therapy areas.\nStrong sense of accountability and urgency; able to prioritize and multitask in changing environments.\nEffective in a matrixed, multicultural setting; fosters culturally sensitive relationships.\nCustomer-focused mindset with high standards of quality and compliance.\nPositive, growth-oriented, self-driven, and professional demeanor aligned with company values.\nEducation and experience\nBachelor’s degree (or higher) with extensive direct site management (monitoring) in bio/pharma/CRO.\nWhat we offer\nOpportunity to shape clinical research at high-performing sites and contribute to global development programs.\nA collaborative environment with growth, mentorship, and continuous improvement.\nCompetitive compensation and benefits.\nHow to apply Please submit your resume/CV and a brief cover letter outlining your relevant monitoring experience and site leadership achievements\nAdditional location(s) Compensation Information:\nRequired Skills:\nAdverse Event Reporting System, Clinical Development, Clinical Research, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Management, Clinical Trial Planning, Clinical Trials Monitoring, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (GCP)Preferred Skills:\nClinical TrialsCurrent Employees apply HERE\nCurrent Contingent Workers apply HERE\nSearch Firm Representatives Please Read Carefully\nMerck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.\nEmployee Status:\nRegularRelocation:\nNo relocationVISA Sponsorship:\nNoTravel Requirements:\nNo Travel RequiredFlexible Work Arrangements:\nRemoteShift:\nNot IndicatedValid Driving License:\nNoHazardous Material(s):\nN/AJob Posting End Date:\n11/7/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.","description_format":"text","description_chars":7032,"description_truncated":false,"requirements":{"experience_years_min":null,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[{"language":"English","level":"Advanced (C1)","optional":false}]},"benefits":["Flexible schedule"],"hiring_locations":[{"name":"United Kingdom","iso":"GB","kind":"country"}],"hiring_excludes":[],"relocation_offered":true,"industries":["Veterinary Medicine","Vaccines","Biologics & Biosimilars","Oncology Therapeutics"],"lifecycle":[{"event":"open","at":"2026-10-22T14:19:30Z"}],"visa":[],"liveness":{"score":84,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.931,"p_room":0.9,"age_days":5,"expected_fill_days":15,"reasons":["conf:5","wave","velocity","win:mid","comp:brand"],"computed_at":"2026-10-28T05:59:10Z"},"pay":null,"html_url":"https://alion.io/job/merck-co-clinical-research-associate-5","json_url":"https://alion.io/job/merck-co-clinical-research-associate-5.json","meta":{"generated_at":"2026-10-29T03:33:03Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":5466,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-10-30T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":3768},"rest":"https://alion.io/mcp/rest/get_company?id=3768"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fmerck-co-clinical-research-associate-5"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Fmerck-co-clinical-research-associate-5"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Fmerck-co-clinical-research-associate-5"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/merck-co-clinical-research-associate-5\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fmerck-co-clinical-research-associate-5"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":3088849}},{"tool":"search_jobs","arguments":{"company":"msd.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":3088849},"note":"people open to offers who fit this vacancy"}],"note":"The same data through MCP tools: https://alion.io/mcp/open needs no sign-in (compact searches, postings, people); https://alion.io/mcp with an Alion account has everything. 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