Clinical Associate Resume

This clinical associate resume example provides key ideas of drafting an effective resume. The various sections in the sample will help you to learn the essential features to make a strong, impressive and effective resume. This sample template is drafted by following the guidelines of effective resume writing. A quick review of the sample will help you to draft a resume that gains an interview call.

A clinical associate is a health care practitioner who performs medical research and helps health care facilities in improving the operating policies and procedures of the organization. The major job responsibilities of a clinical associate is to develop short and long term plans, updating clinical documentations, and recommending improvements in clinical processes and procedures.

Clinical Associate Resume Example

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

Reference:

Will be pleased to provide upon request