Clinical Trial Associate Resume

Before any drug is brought in the market, it has to tested either on human beings or animals. Launching the product without testing and following standard protocols will result in the closure of the company. Hence, pharmaceutical companies hire clinical trial associate. These associates handle all necessary paperwork to conduct the trial and ensure complete integrity in the on-going trial. This allows the researcher to concentrate on their research and develop specif products. A degree in Life Sciences or nursing is preferred for this position. When applying, see that your clinical trial associate resume shows presentations, research, and medical skills to bag a call.

Clinical Trial Associate Resume Example

Career Objective:

To use my clinical research associate skills and experience in maintaining integrity of the trails, and observing human reactions against drugs produced by the company.

Summary of Skills:

• Experienced in assisting on clinical research projects
• Possess strong analytical and communication skills
• Exceptional report drafting and organizational skills
• Ease at multi-tasking and troubleshooting
• Ability to maintain the essence of professional in work
• Familiar with the experimental procedures and medical terminology
• Worked in CTMS (Clinical Trial Management System)

Work Experience:

Clinical Associate
The Medicos Pharma, Forest Park, GA
January 2012 - Present

• Assisting in the designing of clinical trials
• Communicating the findings to the research communities
• Ensuring clinical trails maintain their integrity by following ethical practices and legal regulations
• Recruiting and screening people to participate in clinical trails
• Monitoring people's reactions to medical treatment
• Drafting protocols that describe the methods and procedures of clinical trial
• Conducting pre-clinical test for drugs on animals
• Hiring, training and mentoring junior members
• Visiting testings sites and ensuring standard protocol is followed

Junior Clinical Associate
Falcon Research Group, Forest Park, GA
June 2010 to December 2011

• Implemented trail, documented and communicated changes or concerns to the research community
• Ensured trials are conducted as per ethical and regulatory standards set
• Monitored trail information, sites and production processes
• Analyzed the outcome of the clinical trial and suggested changes
• Verified accuracy, reliability and completeness of the trial reports
• Create a blueprint for trial
• Oversaw standard procedures through the trial process
• Scheduled and maintained total information of clinical trials
• Kept and ordered stock of supplier for the laboratory

Education:

• Bachelor's Degree in Life Sciences
  Hit University, Forest Park, GA
  2009

References:

On request.