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Clinical Research Associate

2+ years
Preferred by CompanY
10 May 2, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life SciencE Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title:

Clinical Research Associate


Company:

Confidential (Global clinical research company, est. 1995, 2,500+ employees)


Location:

Remote (Based in Mexico)


Job Type:

Full-time


About the Company:

A dynamic, global clinical research company established in 1995, employing over 2,500 professionals worldwide. The company is committed to transforming medical science and delivering new treatments to patients. Known for putting people first, it offers strong employee support, growth opportunities, and a collaborative environment.


Job Description / Responsibilities:

  • Conduct site monitoring visits: selection, initiation, routine, and closeout

  • Train investigators, site staff, and internal project teams

  • Handle complex clinical studies

  • Perform CRF review, source document verification (SDV), and query resolution

  • Maintain site communication and management

  • Contribute to site identification and feasibility research

  • Serve as liaison with clinical investigators, vendors, and support services

  • Prepare presentations for Investigator Meetings

  • Participate in and support audits and regulatory inspections

  • Assist Regulatory Affairs in collecting site regulatory documents

  • Use automated tracking systems for study-specific data


Minimum Qualifications:

  • Bachelor’s degree in Medicine

  • At least 2 years’ experience in patient care, healthcare, or clinical setting

  • Fluent in Spanish and English (Full working proficiency)

  • Proficient in MS Office

  • Strong planning, communication, collaboration, and problem-solving skills

  • Willingness and availability to travel


Preferred / Bonus Qualifications:

  • Experience in Clinical Research

  • Interest in mentoring or lead monitor roles in the future


Career Growth Opportunity:

  • Opportunity to grow into senior, trainer, or lead CRA roles

  • Access to tailored courses and mentorship

  • Exposure to complex clinical studies in a dynamic global team