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Clinical Trial Rater - PRN

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 Clinical Trial Rater at Wake Research, an M3 company.  This position is on-site and located in Sandy Springs, GA with possible travel on the east coast.  

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

  • Qualified candidates must have a minimum of 2 years' experience performing psychometric rating scales in a clinical setting or for clinical trials
  • Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills 
  • Strong written and verbal communication skills
  • Ability to multi-task, work under time constraints, and work both independently and cooperatively with interdisciplinary teams
  • Preferred: Current or previous certifications to rate the following scales: SCID-5-CT, MINI, LSAS, HAM-A/D, C-SSRS, MADRS, MGH-ATRQ, ISI, CGI, HDRS-17, PANSS, YMRS, ADAS-Cog, CDR
  • Master’s Degree, Doctor of Medicine, and/or PhD/PsyD in Psychology, Social Work, Psychopharmacology, or related field required

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.

*M3 reserves the right to change this job description to meet the business needs of the organization.

#LI-LB1
#LI-Onsite

Average salary estimate

$70000 / YEARLY (est.)
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$60000K
$80000K

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What You Should Know About Clinical Trial Rater - PRN, M3USA

If you're a passionate mental health professional seeking to find a meaningful role where you can directly contribute to the advancement of clinical research, look no further than the Clinical Trial Rater position at M3 Wake Research in beautiful Sandy Springs, GA. As a Clinical Trial Rater at M3 Wake Research, you’ll play a crucial role in interviewing research participants experiencing various cognitive and behavioral disorders while evaluating their eligibility for groundbreaking studies. Your responsibilities will include communicating with patients and their caregivers, reviewing medical histories, and administering critical psychometric tests as part of your assessment. Your work will adhere to strict protocols and regulatory guidelines, ensuring the highest ethical standards in clinical research. You'll also have the opportunity to participate in ongoing training programs, further developing your professional skills. With a supportive environment that encourages teamwork and innovation, M3 Wake Research is the perfect place to bring your expertise in psychology or a related field to the forefront of clinical trials. Join our mission as we’ve been leading the charge in successful clinical studies since 1984, and be a part of a team that is dedicated to making a difference in the healthcare landscape. Together, we can drive change and improve lives through cutting-edge research.

Frequently Asked Questions (FAQs) for Clinical Trial Rater - PRN Role at M3USA
What are the key responsibilities of a Clinical Trial Rater at M3 Wake Research?

As a Clinical Trial Rater at M3 Wake Research, your primary responsibilities will include interviewing potential research participants and their caregivers, reviewing medical histories, and administering psychometric tests as per study protocols. You’ll also need to stay compliant with guidelines from the FDA, GCP, and HIPAA, ensuring ethical conduct in research.

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What qualifications are required for the Clinical Trial Rater position at M3 Wake Research?

To qualify for the Clinical Trial Rater position at M3 Wake Research, candidates should possess a Master’s Degree or higher in Psychology, Social Work, Psychopharmacology, or a related field, along with a minimum of 2 years of experience in performing psychometric rating scales in a clinical or trial setting. Additional certifications in specific scales are preferred.

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How does M3 Wake Research support the professional development of Clinical Trial Ratters?

M3 Wake Research is committed to your professional growth by offering various ongoing training programs, webinars, and conference calls. As a Clinical Trial Rater, you will receive rater training and Good Clinical Practice (GCP) training to equip you with essential skills and knowledge for success.

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What is the work environment like for a Clinical Trial Rater at M3 Wake Research?

The work environment for a Clinical Trial Rater at M3 Wake Research promotes teamwork and collaboration. Situated in Sandy Springs, GA, you’ll be surrounded by supportive colleagues in a dynamic setting that values innovation and encourages every member to contribute to impactful healthcare advancements.

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Is previous experience needed to apply for the Clinical Trial Rater position at M3 Wake Research?

Yes, candidates applying for the Clinical Trial Rater role at M3 Wake Research should have at least 2 years of relevant experience in psychometric rating or clinical trials. This experience will enable you to effectively handle the responsibilities associated with the role.

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Common Interview Questions for Clinical Trial Rater - PRN
Can you describe your experience with psychometric rating scales?

In your response, emphasize any previous roles where you performed psychometric assessments, discussing specific scales you’ve used. Highlight your understanding of the significance of these scales in clinical trials and mention any training you’ve completed regarding these assessments.

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How do you ensure compliance with regulatory guidelines during interviews?

It's essential to make reference to your familiarity with FDA regulations, GCP, and HIPAA. Discuss the methods you adopt to maintain compliance, such as thorough preparation before interviews and ensuring informed consent from participants.

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What steps do you take to effectively communicate with participants and their caregivers?

Outline your approach to building rapport with participants and caregivers. Include strategies for active listening and being empathetic. You might want to mention any techniques you employ to explain complex information in an accessible way.

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How do you handle challenging situations with participants during assessments?

Describe specific strategies you employ to de-escalate stressful situations, such as staying calm and providing reassurance. Share an example of a past experience where you successfully managed a difficult interaction, demonstrating your problem-solving and interpersonal skills.

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What do you find most rewarding about working in clinical research?

Share your passion for improving lives through research and how it drives your commitment to the field. Discuss the impact of clinical trials on healthcare advancements and how being a Clinical Trial Rater allows you to play an important role in this process.

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Can you give an example of a time you collaborated with a team to achieve a goal?

Provide a specific scenario where your teamwork led to a successful outcome. Highlight your role in communication and collaboration, showcasing your ability to work effectively with interdisciplinary teams.

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How do you prioritize your workload when faced with tight deadlines?

An effective answer will include your time management strategies, such as creating a prioritized task list or using scheduling tools. Discuss how you adapt to changing circumstances while ensuring the quality and integrity of your work.

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What do you know about M3 Wake Research and its mission?

Demonstrate your knowledge about M3 Wake Research, emphasizing its role within the clinical research landscape. Mention its dedication to ethical compliance and commitment to excellence in conducting clinical trials, paralleling it with your values and goals.

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What psychometric tools are you most familiar with, and how have you used them?

List specific psychometric tools, such as CDR, ADAS-COG, or MMSE, and describe your experience administering them. Discuss the context in which you’ve utilized these tools and the importance of accurate data collection in clinical trials.

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How do you stay updated on advancements in clinical research?

Articulate your strategies for staying informed, such as attending webinars, reading relevant literature, or engaging with professional organizations. Illustrate your passion for continuous learning and how it enhances your capabilities as a Clinical Trial Rater.

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Full-time, on-site
DATE POSTED
April 10, 2025

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