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SR CLINICAL RESEARCH COORDINATOR
Description:
• Interacts with co-workers, visitors, and other staff consistent with company values.
• Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP).
• Prepares and submits all materials for the Institutional Review Board (IRB) and other regulatory bodies as required by the protocol to ensure compliance in a timely fashion.
• Maintains accurate subject log, tracks expenses, submits appropriate documentation to Grant Administrator on a monthly basis for payment due for visits on all studies.
• Performs regular quality control assessments to ensure that clinical trial data is collected and stored per GCP.
• Organizes and maintains documentation of all patient data.
• Designs electronic capture databases, if appropriate, and manage all the data collected.
• May provide clerical and technical support to ensure adherence to research protocols and quality of information received.
Additional Skills & Qualifications:
Education: Minimum High School Diploma or equivalent. Bachelor’s Degree. Master’s Degree
Experience: High School Diploma or equivalent and 6 years of clinical research experience and SOCRA CERT required OR Bachelor’s degree and 2 years of clinical research experience OR Master’s Degree and 1 year clinical research experience.
Benefits:
Contact Us:
Please email a copy of your resume and 2-3 professional references to mscherlacher@actalentservices.com
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Other
$60k-80k (estimate)
05/09/2024
05/12/2024
The job skills required for Senior Clinical Research Coordinator include Clinical Research, Clinical Trial, Initiative, Technical Support, etc. Having related job skills and expertise will give you an advantage when applying to be a Senior Clinical Research Coordinator. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Senior Clinical Research Coordinator. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Senior Clinical Research Coordinator positions, which can be used as a reference in future career path planning. As a Senior Clinical Research Coordinator, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Senior Clinical Research Coordinator. You can explore the career advancement for a Senior Clinical Research Coordinator below and select your interested title to get hiring information.