Clinical Rater

This role is with Accellacare, part of ICON'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 better access, greater efficiency, and improved outcomes in clinical research. We are currently seeking a Clinical Rater to join our diverse and dynamic team. As a Clinical Rater at ICON, you will play a key role in conducting structured 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-quality, reliable data that supports the integrity and success of our clinical trials. Title: Clinical Rater Location: 4300 Long Beach Blvd, suite 500, Long Beach, CA 90807 Onsite - Long Beach, CA Job Description: 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 scale scoring. Work closely with data management teams to resolve data queries related to rating scales. Participate in internal training programs related 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, CGI Perform interview/ratings on study subjects to determine current levels of functioning throughout the duration of the study. Follow study specific guidelines for administration of proper scales. Ensure subject safety by appropriately assessing and responding to any potential for harm to self or others and reporting it appropriately. Actively work to maintain consistency in the performance of ratings over time for individual subjects to ensure efficacy and prevent rater drift. Knowledgeable of Diagnostic and Statical Manual for Mental Disorders version 5, 5CR, 5TR and future amendments or revisions. Proficient in conducting diagnostic rating scales, such as the SCID, M.I.N.I, K-Sads. Perform interview/ratings on study subjects to create a clinical impression of the subject’s current psychiatric or cognitive state throughout the duration of the study. Articulate ratings issues to CRO and/or Sponsor, Principal or Sub-Investigator and other members of the study team Maintain accurate, complete, and timely visit source documentation as well as sponsor required information. Complete subject’s clinical intake form (i.e., psychiatric history) and submit to the study team as specified. Assess and complete subject eligibility (i.e. screening forms). Interact with medical monitor regarding subject inquiries. Perform continuous reviews of eligibility criteria (i.e., inclusion and exclusion criteria) for each participant during the screening / randomization period. Verify diagnosis/clinical eligibility for telephone screens and pre-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 Bill of Rights). Become familiar with and adhere to principles of Good Clinical Practices and general ethical guidelines, as related to clinical trials. Become familiar with and adhere to the FDA Regulations pertaining to clinical trials. Review medical history with Clinical Research Coordinator (CRC) information obtained at screening. Review and reconcile medical records received for subjects; prepare Principal Investigator (PI) notes to explain discrepancies, where applicable. Creates tools and assessments to ensure effective training of clinical outcomes assessment raters/interviewers Assist team in management and assessment of adverse events. Qualifications: Minimum of a MD required + 1 years of Rating experience Skill in developing and maintaining effective working relationships with study participants, families, staff and the public Ability to complete paperwork with precision and attention to detail Ability to interpret, adapt and apply guidelines and procedures Ability to work independently as well as functioning as part of a team #LI-Accellacare #LI-SB4 Are you a current ICON Employee? Please click here to apply: link ICON is an award-winning workplace that enables you to make 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 find 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 align with your career goals. Apply tot his job Apply To this Job