{"id":3718751,"url":"https://alion.io/job/merck-co-cra-junior","title":"CRA Junior","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":97,"open_postings":176,"ghost_share":0.034,"stale_share":0.119,"repost_share":0.182,"time_to_fill_p50_days":16,"computed_at":"2026-11-08T05:47:12Z"}},"role":"Biotech","role_family":"Biotech","seniority":"junior","employment_type":"full_time","work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Buenos Aires, Argentina"],"countries":["AR"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":2,"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":"2026-11-03T00:00:00Z","employer_posted_date":"2026-11-03","last_verified_at":"2026-11-08T10:50:28Z","board_verified":true,"closed_at":null,"days_open":5,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":5},"description":"Job Description\nWith support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites.\nDevelops strong site relationships and ensures continuity of site relationships through all phases of the trial.\nPerforms clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.\nGains an in-depth understanding of the study protocol and related procedures.\nCoordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.\nParticipates & provides inputs on site selection and validation activities.\nPerforms remote and on-site monitoring & oversight activities using various tools to ensure:\n- Data generated at site are complete, accurate and unbiased\n- Subjects’ right, safety and well-being are protected\nConducts 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.\nCollects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.\nCommunicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.\nIdentifies, 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.\nWorks in partnership 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\nManages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.\nSupports audit/inspection activities as needed.\nPerforms co-monitoring where appropriate.\nCompetency Expectations:\nFluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand technical information. Developing ability to present technical information with support.\nGood understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.\nGood understanding of Global, Country/Regional CRA Guidelines and ability to work within these guidelines.\nHands on knowledge of Good Documentation Practices\nDeveloping skills in Site Management including management of site performance and patient recruitment\nDeveloping level of monitoring skill and independent professional judgment.\nGood IT skills (Use of MS office, use of some clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices.\nWorks with high quality and compliance mindset.\nCapable of managing complex issues, solution-oriented approach.\nAbility to perform root cause analysis and implement preventative and corrective action.\nBehavioural Competency Expectations:\nEffective time management, organizational and interpersonal skills, conflict management\nAble to work with other experienced research professions to develop skills across multiple protocols, sites and therapy areas.\nHigh sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment, with support from Line Manager.\nWorks effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships.\nDemonstrates commitment to Customer focus.\nPositive mindset, growth mindset, capable of working independently and being self-driven.\nDemonstrates and projects professional demeanor and communication consistent with organizational policies and practices.\nRequirements\nB.A./B.S. required with strong emphasis in science and/or biology.\nMin. 2 years of clinical research experience. Related CR experience may include Clinical Trial Assistant, Study Coordinator, Regulatory CTC or similar.\nAdditional location(s) Compensation Information:\nRequired Skills:\nAccountability, Accountability, Adverse Event Report, Clinical Evaluation Reports, Clinical Reporting, Clinical Research, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials Monitoring, Communication Sciences, Data Analysis, Detail-Oriented, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (GCP), Investigations Training, Key Stakeholder Relationships, On Site Monitoring, Problem Solving, Protocol Adherence, Regulatory Compliance, Research Protocols, Root Cause Analysis (RCA), Site Inspections {+ 6 more}Preferred Skills:\nCurrent 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:\nHybridShift:\nNot IndicatedValid Driving License:\nNoHazardous Material(s):\nnoJob Posting End Date:\n11/10/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. 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