Clinical Research Associate
IQVIA Holdings
Clinical Trial Rater – Borderline Personality Disorder (BPD)Location: Remote based in the US Hours: Approximately 5h per week Role: Clinical SpecialistStart: immediateContract basedIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with top pharmaceutical and biotech companies to accelerate innovation and improve patient outcomes. Our mission is to combine data science and human expertise to transform healthcare worldwide.We are seeking experienced and reliable Clinical Trial Raters to conduct standardized psychiatric assessments for a clinical trial in Borderline Personality Disorder (BPD). The rater will be responsible for administering validated clinician?rated instruments, ensuring high-quality, consistent data collection in accordance with the study protocol, GCP, and regulatory requirements.This role requires strong clinical judgment, experience with psychiatric populations, and the ability to maintain objectivity and inter?rater reliability across multiple assessments and time points.Key ResponsibilitiesConduct structured and semi?structured clinical interviews with trial participants diagnosed with Borderline Personality DisorderAdminister, score, and document validated psychiatric rating scales: CGI-S, and CGI-C or CGIC-SMaintain inter?rater reliability, including participation in calibration, training, and quality review sessionsIdentify and escalate safety concerns (e.g. suicidality) according to protocol and sponsor guidelinesWork closely with study investigators, site staff, and sponsor/CRO teams to support high?quality trial executionAdhere to Good Clinical Practice (GCP), SOPs, and ethical guidelines at all timesMaintain participant confidentiality and a trauma?informed, empathetic approach during all assessmentsRequired QualificationsEducation: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign Medical Doctor (FMD), or Doctor of Osteopathic Medicine (DO)Licensure: Licensed Clinician: MD/FMD/DO, Psychiatrist, Clinical Psychologist, Psychotherapist, Mental Health Counselor/Practitioner (LMHC/LCMHC/LMHP) or Professional Counselor (LPC/LCPC/LPCC)Clinical Experience: 3 years of clinical experience with Borderline Personality Disorder (BPD) populationClinical Trial Rater Experience 3 years of experience as clinical trial rater, including semi-structured psychiatric assessments3 years of experience with Clinical Global Impression rating scalesClinical Global Impression-Severity (CGI-S) andClinical Global Impression-Change (CGI-C) orClinical Global Impression-Change in Severity (CGIC-S)Why Work With Us?Flexible, remote work schedule.Opportunity to contribute to global clinical research.Collaborate with a team committed to improving patient care and advancing science.
$71.9k - $189k
...out visits) in accordance with contracted scope of work and Good Clinical Practice.• Work with sites to adapt, drive, and track subject... ...Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.• i.e., Good Clinical Practice (GCP) and...SuggestedFull timePart timeLocal areaImmediate startWorldwide- ...Montefiore New Rochelle seeks a Research Associate I to oversee multiple clinical trials, acting as a primary contact for patients and study teams. The role involves coordinating with multiple departments to ensure timely completion of trial activities and adherence to...Suggested
- ...Pulse Biosciences is seeking a Senior Clinical Research Associate to manage and monitor soft tissue ablation trials in the U.S. remote setup. The Sr. CRA will support study planning, site startup, patient recruitment, data quality, and regulatory compliance with CFR FDA...SuggestedRemote work
- ...Job Description Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities Participate...Suggested
$60k - $80k
...searching for talented and passionate people who want to help shape the future of veterinary care. About the position The Vet Clinic Implementation Associate at Vetcove is responsible for overseeing the end‑to‑end management of large‑scale projects that enhance the customer...SuggestedHourly payFull timeRemote workHome office$115k - $125k
...Piper Companies is seeking a Clinical Research Associate (CRA) to join a global leader in clinical research and healthcare analysis for a remote permanent position located based out of CST . The Clinical Research Associate (CRA) will travel to sites 8-10 days out of the...Permanent employmentWork at officeRemote work$4,000 - $9,000 per month
...Clinical Research AssociateDotLab is transforming the diagnosis and management of endometriosis, a disease that affects 1 in 10 women worldwide... ...source of pelvic pain.DotLab is seeking a Clinical Research Associate to join our team and support DotLab clinical trials. This...Work at officeRemote workWorldwideFlexible hours- ...Syneos Health, Inc. is seeking a Clinical Monitoring/CRA to support site management, monitoring, and data integrity across sponsor studies in a remote setup. The role emphasizes regulatory compliance and collaboration with cross-functional teams. The position requires...Remote work
$100k - $110k
...Piper Companies is seeking a Clinical Research Associate II to join a global organization within the clinical research and life sciences industry for a remote permanent role with 60-75% travel across the United States. This CRA II will support cardiovascular, CNS, and...Permanent employmentRemote work- ...Montefiore Hudson Valley Collaborative seeks a Research Associate I to manage multiple clinical trials as a patient-facing liaison and trial team lead. You will work with departments hospital-wide to ensure timely completion of trial-related activities, maintaining protocol...
- ...Montefiore Orthopedics is seeking a Research Associate I to oversee multiple clinical trials. You will serve as the main point of contact for patients, families, and study teams, coordinating across hospital departments to ensure timely completion of trial activities....
- ...organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to... .../patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies...Contract workInterim roleLocal areaImmediate startRemote workWork from homeFlexible hours
$71.9k - $169.3k
...and trusted partnerships that help bring breakthrough treatments to patients faster.Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you...Full timePart timeImmediate startWorldwide- ...A healthcare organization is seeking a Research Associate to work with Principal Investigators in clinical research studies. Responsibilities include overseeing data integrity, managing study information, and preparation of research presentations. Candidates should have...
$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Central/East (NY/NJ or TX) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity...Full timeWork experience placementLocal areaRemote workWork visa- Overview Piper Companies is seeking a Clinical Research Associate (CRA) to support oncology-focused clinical trials for a leading organization within the life sciences and pharmaceutical research industry. The Clinical Research Associate (CRA) role is ideal for an experienced...Remote work
- A leading healthcare organization in New York is seeking a Research Associate to oversee clinical trials. The role requires strong clinical research skills, a Bachelor's degree, and GCP training. Responsibilities include managing daily trial activities, ensuring compliance...
- Overview As a clinical research associate (CRA), you are responsible for completing clinical research and administrative tasks for clients. You facilitate documentation for clinical research. As a CRA, you monitor clinical tasks for correct functioning and completion, evaluate...RelocationVisa sponsorship
- ...UT ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment... ...field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes,...Flexible hours
- ...to support General Medicine and Oncology clinical trials across the Northeast ! This role... ...collaborative team and make an impact in clinical research, we\'d love to connect! CRA II ICON is a... ...of experience as a Clinical Research Associate. In-depth knowledge of clinical trial...
- A leading clinical research organization in New York is seeking a Cancer Clinical Trials CRC I to support clinical trial operations under supervision. Responsibilities include data collection, patient recruitment, and managing informed consent processes. Applicants should...
- Mount Sinai Health System in New York, NY is seeking a Clinical Research Associate I to oversee the lifecycle of clinical studies, from site management through study close-out, ensuring compliance with applicable guidelines and SOPs. You will prepare critical study documents...
- ...Medtech, Digital Health Job Functions: Site Monitoring for clinical trials Location: Meditrial USA Inc. 866 United Nations Plaza... ...to travel Meditrial is seeking a certified Clinical Research Associate (CRA) with extensive experience in medical device clinical trials...Interim roleWork at officeLocal areaRemote work
- Kelly Science and Clinical FSP is currently seeking a Regional Clinical Research Associate for a long-term engagement in the US with one of our Global Medical Device clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution...Full time
- ...Responsibilities and Study Conduct Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP)... ...Specialist, Clinical Data Scientist) May Mentor / Train Clinical Research Associates and Sr CRA I as assigned May serve as an SME on related...Local areaRemote workWeekend work
$113k - $153k
Title: Sr. Clinical Research Associate - VahatiCor Status: Full-time, Exempt Reports to: Sr. Clinical Program Manager Overview VahatiCor is a medical device company developing breakthrough cardiovascular technologies, including Class III catheter-based systems. We operate...Permanent employmentFull timeRemote workVisa sponsorshipWork visa- ClinChoice is a global, full-service CRO providing clinical research services to pharmaceutical, biotechnology, medical device and consumer... ...currently seeking an experienced Senior Clinical Research Associate (Senior CRA) to join our in-house team. As a Senior CRA, you...Permanent employmentContract workFor contractorsFreelanceWork at officeLocal areaRemote work
$103k - $130k
Sr. Clinical Research Associate (Sr. CRA) The Sr. Clinical Research Associate (Sr. CRA) is responsible for the set‑up, initiation, execution, monitoring and close‑out of IVD and medical device clinical trials at external clinical research sites and/or laboratories. The...Contract workRemote workNight shift- Senior Clinical Research Associate - Oncology (Myelofibrosis) - East Region What You Will Be Doing Serve as the primary point of contact between investigational sites and the sponsor Conduct all types of site visits, including selection, initiation, routine monitoring...Local areaVisa sponsorshipFlexible hours
- ...position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Sr Clinical Research Associate based in United States. This role offers an opportunity to play a critical part in the successful execution of clinical...Temporary workWork at officeLocal areaRemote workFlexible hours
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