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Senior Clinical Research Associate

0-2 years
Not Disclosed
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:

Senior Clinical Research Associate I


Company:

PSI CRO
A global, privately owned Contract Research Organization founded in Switzerland with nearly 30 years of experience, supporting high-quality clinical trials across a wide range of therapeutic areas. Known for selectivity and high standards, PSI fosters an inclusive and collaborative workplace.


Location:

Hybrid – Almaty, Kazakhstan


Job Type:

Full-time


About the Company:

PSI is a respected CRO that combines global reach with a people-first culture. With operations spanning continents, PSI delivers consistently high-quality clinical trial services, particularly in Phases II and III, including oncology. The company values diversity, inclusivity, and long-term team development.


Job Description / Responsibilities:

  • Conduct and report site monitoring visits (selection, initiation, routine, and close-out)

  • Perform case report form (CRF) reviews, source document verification, and resolve queries

  • Maintain regular communication and oversight of assigned sites

  • Act as a point of contact for vendors and in-house support services

  • Provide updates on study progress to internal project teams

  • Participate in site feasibility assessments

  • Support regulatory submissions and documentation preparation


Minimum Qualifications:

  • Bachelor’s degree in Life Sciences (or equivalent combination of education and experience)

  • Proven independent monitoring experience within Kazakhstan

  • Experience with Phase II/III clinical trials, preferably in Oncology

  • Proficient in English (spoken and written)

  • Skilled in Microsoft Office

  • Strong planning, multitasking, and teamwork abilities

  • Effective communication, collaboration, and problem-solving skills

  • Willingness and ability to travel


Additional Information:

PSI offers a supportive environment where your expertise will be visible and valued. Join a growing team dedicated to clinical excellence, innovation, and career growth.