What are the responsibilities and job description for the Clinical Research Trial Rater - Full-Time position at Wake Research?
Job Description
Job Description
Company Description
M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in the US. M3 Wake Research continues to grow through acquisitions and uncompromising commitment to careful planning and execution in accordance with regulatory compliance.
Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential clinical trial participants across the US. As of today, our board-certified physicians have completed more than 7,000 successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data.
Due to our continued growth, we are hiring for a Trial Rater / Sub-Investigator at Wake Research, an M3 company. This position is on-site and located in Los Alamitos, CA with some travel within CA . This is a full-time, onsite position. The ideal candidate will also be able to function in a Sub-Investigator capacity.
Job Description
The Clinical Trial Rater, a mental health professional, will be solely responsible for interviewing research participants and their informants / caregivers who are being evaluated to participate in a research study for various cognitive and behavior disorders.
Including, but not limited to the following :
- Review patient’s medical history collected by the Wake Research Staff / Clinicians
- Communicates with the patient as well as the patient’s study partner / informant
- The Clinical Trial Rater will administer semi-structured test or rater scales as per protocol, not limited to CDR, ADAS-COG, MMSE, CSSRS, Cognitive Battery Test, ESS, and like exams
- Attend and successfully complete all training programs; participate in ongoing conference calls, webinars, and other professional development opportunities
- Complete provided rater training and Good Clinical Practice (GCP) training
- Conduct interviews following specific study protocols, FDA, GCP, ICH, and HIPAA Privacy guidelines
Qualifications
Requirements :
Additional Information
About M3 :
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.
Benefits
Compensation for this role is $125,000 to $155,000.
All your information will be kept confidential according to EEO guidelines.
LI-Onsite
LI-JD1
Salary : $125,000 - $155,000
