Contract Clinical Research Associate Resume
A contract clinical research associate will have the same responsibilities as her peers on the payroll. She plays a major role in the research trials and assists seniors. Every new product or drugs the company is planning to manufacture, or change the existing one, has to go through a rigorous trial sessions. The CCRA sees that the set guidelines are followed and safety of the people or the animals on whom the trial is done is taken care of. If you are searching for this position, see that you include skills such as research, coordination, organizational, communication, and documentation.
Contract Clinical Research Associate Resume Example
Adam S. Greer
4852 Webster Street
Rahway, NJ 07065
Phone: 732-574-8925
Email: asgreer@freemail.com
Career Objective:
To work as a contract clinical research associate with a reputed clinical research organization and handle the documentation, preparation, and deliverables of trail projects.
Summary of Skills:
- Experience of documenting and assisting in clinical trials research
- Clear, concise, and effective written and verbal communication skills
- Strong organizational, computer, and problem-solving skills
- Thorough knowledge of FDA and GCP principles and regulations
- Strong analytical, research, and trial preparation skills
- Detail-oriented, fast learner, and good listener
Work Experience:
Clinical Research Associate
ABC Pharmaceuticals Inc., Rahway, NJ
June 2012 - Present
- Providing support to the project team and executing additional responsibilities as instructed
- Performing documentation and monitoring of all clinical research trial data
- Updating knowledge of standard protocols for projects
- Assisting on-site inspection and screening people for clinical trials
- Ensuring the site is prepared as per standard protocols and current regulations
- Compiling and verifying completeness of all essential documents necessary to proceed with trials
- Filing, drafting, submitting, retrieving and reviewing case reports
- Attending trainings, meetings, and teleconferencing as required
Junior Clinical Research Associate
Saint Percept Medicine Group, Rahway, NJ
November 2010 - May 2012
- Assisted in the trial of cardiovascular and diabetes drugs
- Reviewed and corrected discrepancies in clinical research data
- Oversaw laboratory activities of multiple clinical trial sites
- Examined regulatory documents and monitoring reports
- Ensured trials are conducted in compliance with regulatory standards set
- Communicated and documented every single step taken in the trial
- Established and maintained trial master files in digital and physical formats
- Provided administrative support and trial scheduling
Education:
- Bachelor's Degree in Pharmacy
Rahway University, Rahway, NJ
2010
Reference:
On request.
