Clinical Associate Resume

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Contact Address: [street]

[Country] [City] [State/Province] [Zip Code]

Contact Number: (012)-345-6789

Email Address: [[email protected]]

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Career Objective:

To work as a clinical associate and utilize my over 4 years of experience in helping the organization improve its operation policies and procedures so that better care to patients can be provided without any hassles.

Core Competencies:

  • Comprehensive knowledge of drug development processes and clinical study budgeting
  • Familiar with clinical practices, clinical research ethics, ICH guidelines, FDA CFR, pharma codes, and other applicable local regulations
  • Extensive knowledge of clinical subjects, specimens and clinical trial design
  • Possess effective communication skills and has the ability to maintain confidential information

Work Experience:

Organization: The Medicos Pharma, Georgina
Duration: January 2012 – Present
Designation: Clinical Associate

  • Responsible for conducting site-level of clinical trials set forth in the protocol, patient recruitment and retention, feasibility, site monitoring, investor obligations and general compliance
  • Handle the tasks of ensuring that the integrity and quality of data collected in the organization sponsored clinical trails
  • Perform responsibilities of ensuring adequate protection of the rights of all subjects involved in company sponsored clinical trials
  • Responsible for performing activities within project timelines, priorities, and productivity specification
  • Perform clinical research by adhering the local laws and regulations governing the principles of conducting clinical research
  • Responsible for leading therapeutic teams and other clinical based development operations functions
  • Perform work activities in compliance with ICH, Pharma, and CFR guidelines and procedures

Organization: Clinical Research Group, Georgina
Duration: June 2010 – December 2011
Designation: Junior Clinical Associate

  • Responsible for assisting with preparation of all external and internal documentation for assigned trials
  • Perform the tasks of organizing and preparing study files related to the findings of clinical study
  • Handle responsibilities of maintaining and tracking revisions to all clinical documents like case report forms and patient informed consent forms for accuracy
  • Responsible for supporting clinical project manager and clinical associate in ensuring compliance with the protocols f clinical study
  • Perform the tasks of tracking delivery and receipt of required materials and supplies as well as provide status updates to the clinical manager

Educational Summary:

Achieved Bachelor’s degree in Life Science
Information Technology Center, Georgina in the year 2009


Will be pleased to provide upon request