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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.