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.
The following entry-level resume sample for a CRA position provides a solid foundation for graduates looking to enter the clinical research field, showcasing educational background, relevant experience, and key competencies in a professional format suitable for a beginner’s resume.
Entry Level CRA Resume Sample 1
Jane Doe
1234 Maple Lane
Seattle, WA 98101
(123) 456-7890
janedoe @ email . com
CLINICAL RESEARCH ASSOCIATE
OBJECTIVE
Detail-oriented and meticulous individual, holding a Bachelor’s Degree in Life Sciences, eager to apply theoretical knowledge in a practical environment. Looking to leverage skills in trial design and data integrity at XYZ Pharmaceuticals to aid in the successful execution of clinical research and trials.
HIGHLIGHTS OF QUALIFICATIONS
• Strong understanding of clinical trial protocols and compliance requirements.
• Proficient in data collection, verification, and analysis ensuring high data integrity.
• Excellent organizational skills with the ability to manage multiple tasks efficiently.
• Strong communication skills, capable of effectively coordinating with teams and managing stakeholder relationships.
CORE COMPETENCIES
• Study Protocol Adherence
• Clinical Research Regulations
• Data Management
• Ethical Compliance
• Patient Interaction
• Detail-Oriented Documentation
• Problem-Solving Abilities
• Team Collaboration
EDUCATION
Bachelor’s Degree in Life Sciences
University of Washington, Seattle, WA – 2023
RELEVANT PROJECTS
Undergraduate Research Assistant
University of Washington, Seattle, WA
Jan 2022 – Dec 2023
• Supported the research team in the design and implementation of study protocols.
• Contributed to the preparation and submission of regulatory documentation.
• Assisted in the collection and analysis of research data, ensuring compliance with ethical standards.
• Participated in meetings and presented findings to peers and supervising faculty.
VOLUNTEER EXPERIENCE
Volunteer
Health Right Clinic, Seattle, WA
June 2021 – August 2021
• Provided administrative support in patient record management.
• Assisted healthcare professionals in patient care and data recording.
• Played a key role in organizing health awareness camps, and enhancing community engagement.
ADDITIONAL SKILLS
• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint)
• Basic knowledge of SAS and SPSS software
• Effective communication and interpersonal skills
AWARDS & HONORS
• Dean’s List for Academic Excellence, 2021-2023
• Recipient of the College Scholar Award for Outstanding Undergraduate Research
Entry Level Clinical Research Associate Resume Sample 2
Frank Lone
585 6th Street
Cleveland, OH 88581
(000) 591-3729
franklone @ email . com
CLINICAL RESEARCH ASSOCIATE
OBJECTIVE
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.
HIGHLIGHTS OF QUALIFICATIONS
• 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.
SPECIAL KNOWLEDGE
• Timelines Management
• Regulatory Compliance
• Practice Harmonization
• Intervention Plans
• Investigator Selection
• Trial Monitoring
• Data Verification
• Technical Trial Reports
• Study Documentation
EDUCATION
Bachelor’s Degree in Life Sciences
Cleveland Technical College, Cleveland, OH – 2024
INTERNSHIP EXPERIENCE
Intern
Blue Lab, Cleveland, OH
Sep 2022 – Jan 2024
• 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 issued 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
AWARDS & HONORS
• Awarded appreciation letter for immense contribution to the life sciences lab through voluntary summer services.
• Chosen as the teacher’s assistant for 55 students, owing to exceptional participation in class and special projects.