The Clinical Research Coordinator (CRC)/Rater is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities, performs psychometric rating scales, and plays a critical role in the conduct of the study.
Essential Duties and Responsibilities:
- Assisting trial Investigator in screening and review of potential study participants eligibility
- Administering semi-structured test or rater scales as per protocol, not limited to CDR, ADAS-COG, MMSE, CSSRS, Cognitive Battery Test, ESS, and like exams
- Complete provided rater training and Good Clinical Practice (GCP) training
- Conduct interviews following specific study protocols, FDA, GCP, ICH, and HIPAA Privacy guidelines
- Maintaining case report forms, charts and documentation
- Mentoring, training, and high-level oversight of other clinical research coordinators and research assistants
- Ensuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements
- Collecting and entering data as necessary
- Assist management with potential new hire selection and shadowing process.
- Assist with study start-up, maintenance, and close-out of studies as needed for those on the team
- Ability to be flexible with study assignments
- 2 years' experience performing psychometric rating scales in a clinical setting or for clinical trials (neuro trial experience preferred)
- Clinical skills, including the ability to perform phlebotomy is preferred
- Extensive clinical trial knowledge through education and/or experience
- Successful completion of GCP Certification and Advanced CRC preferred
- Minimum 1-2 years of clinical research coordinator experience required
- Excellent communication and organizational skills
- Detail-oriented
- Familiarity with the Code of Federal Regulations as they pertain to human subject protection
- Strong interpersonal skills
- Strong computer skills
*This position offers compensation of $25/hr - $40/hr.
A career opportunity with M3 Wake Research offers competitive wages, and benefits such as:
- 401(k), 401(k) matching
- Dental insurance
- Disability insurance
- Employee assistance program
- Flexible spending account
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
About M3USA
M3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals, and more. Since our inception in 2000, we’ve seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems.
Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement, and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements.
Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation, shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA.
*M3 reserves the right to change this job description to meet the business needs of the organization
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