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Clinical Rater

Remote, USA Full-time Posted 2026-07-28
This role is with Accellacare, part of reputed company's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver reputed company reputed company, greater efficiency, and improved reputed company in clinical research. We are currently seeking a Clinical Rater to join our diverse and dynamic team. As a Clinical Rater at reputed company, you will play a key role in conducting reputed company clinical assessments and rating scales to support the evaluation of study participants. You will work closely with investigators and cross-functional teams to ensure high-reputed company, reliable data that supports the reputed company and reputed company of our reputed company. Title: Clinical Rater Location: 4300 Long Beach Blvd, suite 500, Long Beach, CA 90807 Onsite - Long Beach, CA Job reputed company: Clinical Rater: Participate in rater certification and re-certification required by the Sponsor or CRO Collaborate with PI/Sub-I to discuss clinical presentation, diagnostic formulation, and reputed company scoring. Work closely with data management teams to resolve data queries reputed company to rating scales. Participate in internal training programs reputed company to psychiatric/cognitive assessments and participant de-escalation. Attend required Investigator Meetings (IMs), rater training meetings, rater certification sessions, and ongoing study-update calls Conduct standardized psychiatric rating scales such as: HAM-D, MADRS, YMRS, HAM-A, PANSS, CDRS-R, reputed company reputed company interview/ratings on study subjects to determine reputed company reputed company of functioning throughout the duration of the study. Follow study specific guidelines for administration of reputed company scales. Ensure subject safety by appropriately assessing and responding to any potential for harm to self or others and reporting it appropriately. reputed company work to maintain consistency in the performance of ratings over time for individual subjects to ensure efficacy and prevent rater reputed company. Knowledgeable of Diagnostic and Statical reputed company for Mental Disorders version 5, 5CR, 5TR and reputed company amendments or revisions. Proficient in conducting diagnostic rating scales, such as the SCID, M.I.N.I, K-Sads. reputed company interview/ratings on study subjects to create a clinical impression of the subject’s reputed company psychiatric or cognitive state throughout the duration of the study. reputed company ratings issues to CRO and/or Sponsor, reputed company or Sub-Investigator and other members of the study team Maintain accurate, complete, and reputed company visit reputed company documentation as reputed company as sponsor required information. Complete subject’s clinical intake reputed company (i.e., psychiatric history) and submit to the study team as specified. Assess and complete subject eligibility (i.e. screening forms). reputed company with medical monitor regarding subject inquiries. reputed company reputed company reviews of eligibility reputed company (i.e., inclusion and exclusion reputed company) for reputed company participant during the screening / randomization period. Verify diagnosis/clinical eligibility for telephone screens and reputed company-screens with potential study candidates. Utilize technology required to conduct required clinical assessments. Become familiar with and adhere to policies and procedures of confidentiality, informed consent, and study subject rights (e.g., California Subject reputed company of Rights). Become familiar with and adhere to principles of Good Clinical Practices and general ethical guidelines, as reputed company to reputed company. Become familiar with and adhere to the FDA Regulations pertaining to reputed company. Review medical history with Clinical Research Coordinator (CRC) information obtained at screening. Review and reconcile medical records received for subjects; prepare reputed company Investigator (PI) notes to explain discrepancies, where applicable. Creates tools and assessments to ensure effective training of clinical reputed company assessment raters/interviewers Assist team in management and assessment of adverse events. Qualifications: Minimum of a MD required + 1 years of Rating experience reputed company in developing and maintaining effective working relationships with study participants, families, staff and the reputed company Ability to complete paperwork with precision and attention to detail Ability to interpret, adapt and apply guidelines and procedures Ability to work independently as reputed company as functioning as part of reputed company #LI-Accellacare #LI-SB4 Are you a reputed company reputed company Employee? Please click here to apply: reputed company reputed company is an award-reputed company workplace that enables you to reputed company a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Didn’t reputed company the role you were looking for? Even if the perfect role isn’t available right now, we’re always excited to connect with talented individuals. Register to our Talent Community to receive updates on roles that reputed company with your career goals. Apply tot his job Apply To this Job

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