CRA (Level I)
Are you a detail-oriented individual with a passion for clinical research? Do you thrive in a fast-paced and dynamic environment? Thermo Fisher Scientific is seeking a highly motivated Clinical Research Associate (Level I) to join our team. As a CRA at Thermo Fisher Scientific, you will play a crucial role in ensuring the success of clinical trials by conducting site visits, monitoring data, and ensuring compliance with protocols and regulations. This is an exciting opportunity for someone looking to launch their career in the field of clinical research. If you have a Bachelor's degree in a related field and excellent communication and organizational skills, we encourage you to apply for this position. Join us in our mission to improve the health and well-being of people around the world through innovative and high-quality products and services.
Conduct site visits to monitor the progress of clinical trials and ensure compliance with protocols and regulations.
Collect and review data and documents from clinical trial sites.
Coordinate with study sites and investigators to ensure timely completion of trial activities.
Communicate any issues or concerns to the project team and work together to find solutions.
Maintain accurate and up-to-date documentation of all clinical trial activities.
Ensure adherence to Good Clinical Practices (GCP) and other applicable regulations.
Participate in the development and review of study protocols and study-related documents.
Assist with the preparation and submission of regulatory documents.
Collaborate with cross-functional teams to support the successful execution of clinical trials.
Identify and report any deviations or adverse events to the appropriate parties.
Stay current with industry trends and regulations related to clinical research.
Participate in training and development opportunities to enhance job knowledge and skills.
Proactively identify and address any potential issues or risks that may impact the success of the clinical trial.
Maintain confidentiality of all study-related information.
Foster a positive and collaborative team environment.
Represent the company in a professional and ethical manner at all times.
Support the company's mission to improve the health and well-being of people around the world.
Adhere to all company policies and procedures.
Complete all assigned tasks and responsibilities within the given timelines.
Continuously strive for excellence and contribute to the growth and success of the company.
Thermo Fisher Scientific is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Conduct site visits to monitor the progress of clinical trials and ensure compliance with protocols and regulations.
Collect and review data and documents from clinical trial sites.
Coordinate with study sites and investigators to ensure timely completion of trial activities.
Communicate any issues or concerns to the project team and work together to find solutions.
Maintain accurate and up-to-date documentation of all clinical trial activities.
Ensure adherence to Good Clinical Practices (GCP) and other applicable regulations.
Participate in the development and review of study protocols and study-related documents.
Assist with the preparation and submission of regulatory documents.
Collaborate with cross-functional teams to support the successful execution of clinical trials.
Identify and report any deviations or adverse events to the appropriate parties.
Stay current with industry trends and regulations related to clinical research.
Participate in training and development opportunities to enhance job knowledge and skills.
Proactively identify and address any potential issues or risks that may impact the success of the clinical trial.
Maintain confidentiality of all study-related information.
Foster a positive and collaborative team environment.
Represent the company in a professional and ethical manner at all times.
Support the company's mission to improve the health and well-being of people around the world.
Adhere to all company policies and procedures.
Complete all assigned tasks and responsibilities within the given timelines.
Continuously strive for excellence and contribute to the growth and success of the company.
Thermo Fisher Scientific is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.