Entry Level CRA (Clinical Research Associate) Resume Sample

Updated on: January 7, 2022

An entry-level resume for a clinical research associate or CRA position is not much different from one where experience is the main focus.

However, you do need to keep a few things in mind when writing an entry-level resume. For one, you are a newbie to the employment world. Your first impression counts immensely.

Secondly, since you do not have the benefit of experience or work-related accomplishments, it might be a bit difficult to make an impactful impression.

Nonetheless, your best efforts are required when creating a resume for an entry-level position.

You may be new to the employment world, but there must be something in your background that makes it easy for you to write a resume with pride.

Looking for a sample? Here is one:

Entry Level CRA Resume Sample (No Experience)

Frank Lone
585 6th Street
Cleveland, OH 88581
(000) 591-3729
franklone @ email . com


Self-motivated, and visionary individual with a deep interest in developing and writing trial protocols to outline the purpose and methodology of each trial. Eager to work for ABC Company to prepare integrated medical reports and design and set up correlating study centers.

• Competent in reviewing study requirements by conducting pre-study visits and drafting evaluation reports.
• Highly skilled in ensuring the quality of clinical trial projects by efficiently verifying materials and data integrity.
• Well-versed in assessing trial sites and personnel and ensuring consent with patient consent processes.
• Adept at drafting appropriate intervention plans to avoid redundant errors and deviations.

• Timelines Management
• Regulatory Compliance
• Practice Harmonization
• Intervention Plans
• Investigator Selection
• Trial Monitoring
• Data Verification
• Technical Trial Reports
• Study Documentation

Bachelor’s Degree in Life Sciences
Cleveland Technical College, Cleveland, OH – 2022


Blue Lab, Cleveland, OH
Sep 2021 – Jan 2022
• Assisted in designing, implementing, and monitoring clinical trials
• Helped in preparing integrated medical and periodic reports, in addition to reviewing and submitting case report forms
• Assessed trail sites and personnel while ensuring that the quality of collected data complied with set protocols
• Supported the drafting of intervention plans for the avoidance of redundancies or data errors
• Documented site visits and created and issues reports and follow-up documents
• Assisted in identifying potential investigators and facilitating effective communication among investigative sites and participants
• Provided support in closing down study centers upon completion of study trials

• Awarded appreciation letter for immense contribution to the life sciences lab through voluntary summer services.
• Chosen as the teacher’s assistant from 55 students, owing to exceptional participation in class and special projects.