Clinical Research Associate Resume

A clinical research associate helps in the preparation, design, implementation, planning and review of a clinical trial to make sure that it holds the ethical and regulatory standards. He also helps in communicating findings to the research community.

The field of clinical research is rapidly expanding field, which has creating many exciting opportunities for the trained professionals. Clinical research associate can get jobs in research industries and hospital sectors and can advance to management role. Also they can also work in broad range of research settings such as:

Government agencies and departments
Contract research organizations
Academic health centers
Private companies, such as biotechnology, pharmaceutical, and medical device firms

Sample Clinical Research Associate Resume

Richard Anderson
1234, West 67 Street,
Carlisle, MA 01741,
(123)-456 7890.

Objective:

Seeking for the position of Clinical Research Associate in the medical field while merging into a globally focused organization that will purposefully utilize my qualifications while offering several opportunities to integrate personal enrichment with professional goals.

Summary of Qualifications:

Deep knowledge of monitoring procedures.
Detailed knowledge of GCP and ICH guidelines including basic understanding o regulatory requirements.
Comprehensive knowledge of Covance S.O.P.'s for site monitoring.
Basic knowledge of clinical trial process.

Skills:

Able to work under optimal supervision
Excellent organization, planning and problem solving abilities.
Excellent negotiation and analytical skills.
Established interpersonal and communication skills.
Fluent in English and other local office languages both verbal and written.
Proficiency in computer.
Able to work effectively and efficiently in a matrix environment.

Employment:

Quintiles Transnational, East Point, FL
Clinical Research Associate

Ensuring the implementation of project plans as assigned.
Responsible for site monitoring, site management, site administration and registry management for clinical studies according to GCP, ICH Guidelines, and Covance Standard Operating Procedures.
Acted as Lead CRA or Local Project Coordinator in projects as assigned.

Adecco Personnel Limited, Halifax, FL
Clinical research Associate

Monitor the clinical trial progress ensuring that it is recorded, conducted and reported in accordance with Standard Operating procedures (SOPs), protocol, Good Clinical Practice (GCP), and the relevant regulatory requirements. Provided study training and administer protocol to assigned site.

Education:

Florida State University College of Medicine, FL
Degree in Science with major in life sciences.

Certifications:

CRA/Quality Assurance Monitor 2005

Clinical Research Coordinator 2005

Certified Mohs Laboratory Technician 1992

Certified Cryostat Technician 1992

Certified CPR 1988 to present

Certified Medical Assistant 1988

Certified Mohs Surgical Technician 1988

Certified Dermatological Surgical Technician 1988