What are the responsibilities and job description for the Clinical Rater position at NextPhase Research Florida?
We are seeking an experienced Clinical Research Rater to join our CNS research team. This position is ideal for a mental health professional with strong clinical interviewing skills and experience assessing psychiatric populations, particularly individuals with conditions such as major depressive disorder, bipolar disorder, schizophrenia, PTSD, and other CNS/psychiatric disorders.
Candidates with experience administering psychiatric rating scales such as MADRS, HAM-D, PANSS, MINI, SCID, YMRS, BPRS, and C-SSRS are strongly encouraged to apply.
Job Description:
The Clinical Rater is responsible for conducting diagnostic interviews and administer psychometric, efficacy, safety, and cognitive assessments for participants enrolled in clinical research studies.
Responsibilities:
- Conduct psychiatric diagnostic interviews and clinical assessments with research participants.
- Administer and score psychiatric rating scales and assessments, including MADRS, HAM-D, PANSS, MINI, SCID, YMRS, BPRS, C-SSRS, and other protocol-specific scales.
- Assess participants' psychiatric symptoms and level of functioning throughout clinical trials.
- Administer neurocognitive battery in subject with different CNS indications.
- Complete subject’s clinical intake forms (i.e. psychiatric history) and submit to the study team as specified.
- Assess and complete subject eligibility/screening forms and interact with medical monitor regarding subjects inquiries.
- Conduct telephone screens and pre-screen with potential study candidates.
- Become familiar with and adhere to policies and principles of confidentiality, informed consent and study subject rights.
- Become familiar with and adhere to the principles of Good Clinical Practices and general ethical guidelines, as related to clinical trials.
- Become familiar with the FDA Regulations pertaining to clinical trials.
- Review medical history with CRC information obtained at screening.
- Review and reconcile medical records received for subjects and prepare PI notes to explain discrepancies, if needed.
- Complete Study Guides and Study Launch with CRC.
- Assist team in management and assessment of adverse events.
- Ensure safety of subjects.
- Assist with recruitment efforts.
- Provide guidance and mentorship to research staff when appropriate.
Knowledge, Skills & Abilities
- Knowledge of medical terminology
- Working knowledge of DSM-5 diagnostic criteria and psychiatric medications
- Working knowledge of technology
- Familiarity with the Microsoft Office Suite
- Excellent organizational skills to independently manage workflow
- Ability to multi-task and prioritize appropriately
- Meticulous attention to detail
- Skill in developing and maintaining effective working relationships with study subjects, families, staff and the public
- Ability to react calmly and effectively in emergency situations
- Ability to interpret, adapt and apply guidelines and procedures
- Bilingual strongly preferred.
Education & Experience
- Doctoral degree in Psychology (PhD/PsyD), Medical Doctor or Foreign Medical Graduate in Psychiatry or similar preferred. Master degree in psychology related field will be considered.
- Two years of clinical experience with psychiatric population
- One year of experience working in clinical research preferred
About Us: Driven by decades of clinical research excellence, we are dedicated to shaping the future of medicine. By combining proven expertise, innovative technology, and compassionate, patient-centered care, we support the discovery and refinement of new therapies. Our mission is to accelerate meaningful progress and deliver better outcomes today and for generations to come.