
Sr Clinical Research Associate
At Thermo Fisher Scientific, we are looking for an experienced, motivated Senior Clinical Research Associate (Sr CRA) to join our dynamic team. The Sr CRA will be a key player in the successful execution of clinical trials from start to finish. The Sr CRA will be responsible for ensuring effective coordination of all activities related to clinical trials, monitoring visits, and data collection.The ideal candidate should have a Bachelor’s degree in a health sciences field and a minimum of three years of on-site clinical trial experience. The successful candidate must be highly organized, detail-oriented, and able to handle multiple tasks simultaneously. He/She must have strong verbal and written communication skills and the ability to work independently in a fast-paced environment.The Sr CRA must be knowledgeable of applicable GCP guidelines and regulations and have a working knowledge of Good Clinical Practices (GCP). Experience in ICH GCP, 21CFR Part 11, and FDA regulations is preferred. The Sr CRA must also possess the ability to work with minimal supervision and demonstrate excellent problem-solving skills.At Thermo Fisher Scientific, we are committed to creating an inclusive environment that celebrates the diversity of our employees and fosters an environment of collaboration and trust. If you are passionate about delivering quality in the clinical trial process and believe you have the experience and qualifications to be our next Sr CRA, we invite you to apply today!
Responsibilities of the Senior Clinical Research Associate:
- Ensure effective coordination of all activities related to clinical trials, monitoring visits, and data collection.
- Adhere to applicable GCP guidelines and regulations and have a working knowledge of Good Clinical Practices (GCP).
- Maintain up-to-date knowledge of ICH GCP, 21CFR Part 11, and FDA regulations.
- Work with minimal supervision and demonstrate excellent problem-solving skills.
- Manage multiple tasks simultaneously in a fast-paced environment.
- Utilize strong verbal and written communication skills to interact with internal and external stakeholders.
- Maintain a high degree of attention to detail and organizational skills.
- Participate in the development and review of clinical trial documents and reports.
- Monitor and review data collected during clinical trials.
- Assist in the development and implementation of clinical trial protocols and procedures.
Good Communication Skills
Ability To Work Independently And As Part Of A Team
Degree In A Scientific Discipline
Knowledge Of Good Clinical Practice (Gcp) And Clinical Trial Regulations
Experience In Clinical Trial Management
Understanding Of Laboratory And Scientific Procedures
Ability To Analyze And Interpret Clinical Data
Good Organizational And Time Management Skills
Documentation
Project Management
Data Analysis
Communication
Database
Auditing
Compliance
Monitoring
Coordinating
Problem-Solving
Negotiating
Regulatory
Assessing
Investigating
Clinical
Communication
Leadership
Time management
Interpersonal Skills
creativity
Organization
Critical thinking
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Sr Clinical Research Associate in Cincinnati, OH, USA is $78,000 - $121,000 per year. The salary range can vary depending on the experience of the applicant and the organization that they are working for. Additionally, the city and state in which the job is located can also affect the salary range.
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Thermo Fisher Scientific is a U.S.-based provisioner of scientific instrumentation, reagents and consumables, and software and services to healthcare, life science, and other laboratories in academia, government, and industry.

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