CLINICAL TRIAL ADMINISTRATOR SKILLS, EXPERIENCE, AND JOB REQUIREMENTS

Published: July 17, 2024 - The Clinical Trial Administrator is equipped with extensive experience in managing regulatory aspects of clinical trials, conducting research protocols, and coordinating with Institutional Review Boards. This role demands strong proficiency in database management, report generation, and a thorough understanding of regulatory policies, enhanced by a professional background in healthcare or scientific fields. The position requires excellent communication, organizational skills, and the capability to function effectively both individually and as part of a diverse research team.

Essential Hard and Soft Skills for a Standout Clinical Trial Administrator Resume
  • Regulatory Compliance Knowledge
  • Protocol Management
  • Data Analysis
  • Report Generation
  • Database Management
  • Statistical Software Proficiency
  • Medical Writing
  • Clinical Monitoring
  • Quality Assurance Techniques
  • Electronic Data Capture Systems
  • Attention to Detail
  • Communication Skills
  • Problem Solving
  • Time Management
  • Teamwork
  • Adaptability
  • Ethical Judgment
  • Critical Thinking
  • Leadership
  • Stress Management

Summary of Clinical Trial Administrator Knowledge and Qualifications on Resume

1. BS in Clinical Research Administration with 5 years of Experience

  • Administrative work experience, preferably in an international settings
  • CTA working experience within pharma/CRO/NHS or Academia
  • Strong written and verbal communication skills
  • Excellent attention to detail
  • Advanced English, full working proficiency in Serbian
  • Good organizational and planning skills
  • Detail-oriented, able to multi-task and work effectively in a fast-paced environment
  • Good problem-solving abilities, flexibility
  • Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects
  • Proficient user of standard MS Office applications (Word, Excel and PowerPoint)

2. BS in Biomedical Science with 3 years of Experience

  • Relevant CTA work experience
  • Working experience in science/research-related field
  • Experience working in clinical trials
  • Have familiarity with clinical trial methodology and GCP
  • Recent experience with Trial master files (TMFs)
  • Strong written and verbal communication skills
  • Must have computer literacy (e.g., Microsoft Word, Excel, PowerPoint, Outlook)
  • Ability to manage multiple tasks and follow up on resolution
  • Team player with a positive attitude
  • Excellent problem-solving and organizational skills

3. BS in Healthcare Administration with 2 years of Experience

  • Working experience in a similar role with an emphasis in Life Sciences
  • Relevant work experience in a global pharmaceutical company/CRO
  • Effective communication skills
  • Computer proficiency (Windows environment)
  • Proficient in Information Technology
  • Be highly organized and efficient
  • Ability to communicate effectively and people-oriented personality
  • Must have a good level of English
  • The ability to organize and prioritize
  • Able to produce work in teams and within a multi-disciplinary environment

4. BS in Nursing with 4 years of Experience

  • Strong experience in global clinical study environment within SP or Pharmaceutical company.
  • Knowledge of the clinical study environment with a strong theoretical or practical administrative organization.
  • Good knowledge of the Good Clinical Practices (GCP) or other clinical study regulations
  • Knowledge of Pharmaceutical Industry R&D and/or GMA
  • Related work experience and training
  • Basic Financial Knowledge
  • Must have a strong English intermediate-level
  • Good written and oral understanding 
  • Ability to work in a strongly regulated environment within a quality management system (QMS)
  • Advanced knowledge of software applications (including Word, Excel, PowerPoint, Adobe Reader, etc.)

5. BS in Public Health with 3 years of Experience

  • Working experience as a CTA in other CRO companies.
  • Administrative work experience, preferably in an international setting
  • Prior experience in Clinical Research
  • Fluency in English and Mandarin
  • PC skills to be able to work with MS Word, Excel and PowerPoint
  • Ability to plan, multitask, and work in a dynamic team environment
  • Strong communication and collaboration skills
  • Experience with eTMF and essential documents.
  • Must have previous experience working in Clinical Operations with knowledge of computer applications.
  • Organized with the ability to meet strict timelines.

6. BS in Biology with 5 years of Experience

  • Experience with regulatory aspects of clinical trials.
  • Experience with conducting and carrying out protocols and research coordination.
  • Familiarity with IRB interaction, regulatory policies, database input and report generation.
  • Research experience in an academic health center with exposure to a team research environment at all levels (senior investigators, nurses, research coordinators, lab technicians.
  • Professional Certificate/NITEC or Diploma in a healthcare or scientific concentration
  • Excellent verbal and written communication skills
  • Strong computer skills and familiarity with relational databases and reporting tool
  • Meticulous and possesses excellent organizational skills
  • Ability to work both independently and in a team
  • Relevant working experience in clinical trials
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