Clinical Research Monitor
WCM-Q
Position Summary The Clinical Research Monitor, under the guidance of the Assistant Director of Human Research Compliance, will assist in the implementation and day-to-day operations of all quality assurance and improvement initiatives for WCM, including audits, Data Safety Monitoring Board, and education programs. Job Responsibilities Participates in the oversight and monitoring of investigator/coordinator compliance with IRB and institutional requirements and the approved protocol. Plans, conducts, and reports internal quality audits, both routine and for-cause, to assure adherence to local and federal requirements Categorizes findings and determines when findings require immediate remedial action; tracks and follows-up on corrective and preventive action to ensure continuing data integrity and operational compliance Provides evaluations and summaries of compliance activities to the Assistant Director, and/or stakeholders within the HRPP Assists with compliance training initiatives including coordinating educational sessions, writing and editing compliance manuals, and developing presentations Oversee procedures with regard to performing data management activities, maintain and update computerized databases, create forms, conduct database searches and create reports for various departments listing current research protocols. Maintain records and prepare correspondence relating to problems for the DSMB and the IRB. Conduct preliminary reviews of all IRB protocols that request the use of DSMB and forward to the chair for initial review of the Data Safety Monitoring Plan. Acts as the WCM DSMB liaison to provide assistance and information to CTSC administrators with regard to the WCM DSMB and adverse event/Unanticipated Problems reporting and procedures. Serve as ESCRO administrator Education Bachelor's Degree in related field Experience Minimum of three years related work experience. Extensive technical knowledge of the functioning of IBCs, DSMBs and IRBs, including extensive knowledge of the technical requirements of the federal regulations that govern human subjects research, adverse events reporting, state laws governing research, and WCMC policies. Knowledge, Skills and Abilities Proficient in word processing and database applications. Knowledge of Data Safety Monitoring Board (DSMB) operations. Prior monitoring/auditing experience. Strong analytical and problem solving skills, excellent interpersonal and communications skills, highly organized and ability to act as a role model for staff. Licenses and Certifications Working Conditions/Physical Demands Cornell welcomes students, faculty, and staff with diverse backgrounds from across the globe to pursue world-class education and career opportunities, to further the founding principle of “any person, any study.” No person shall be denied employment on the basis of any legally protected status or subjected to prohibited discrimination involving, but not limited to, such factors as race, ethnic or national origin, citizenship and immigration status, color, sex, pregnancy or pregnancy-related conditions, age, creed, religion, actual or perceived disability (including persons associated with such a person), arrest and/or conviction record, military or veteran status, sexual orientation, gender expression and/or identity, an individual’s genetic information, domestic violence victim status, familial status, marital status, or any other characteristic protected by applicable federal, state, or local law. Cornell University embraces diversity in its workforce and seeks job candidates who will contribute to a climate that supports students, faculty, and staff of all identities and backgrounds. We hire based on merit, and encourage people from historically underrepresented and/or marginalized identities to apply. Consistent with federal law, Cornell engages in affirmative action in employment for qualified protected veterans as defined in the Vietnam Era Veterans’ Readjustment Assistance Act (VEVRRA) and qualified individuals with disabilities under Section 503 of the Rehabilitation Act. We also recognize a lawful preference in employment practices for Native Americans living on or near Indian reservations in accordance with applicable law. #J-18808-Ljbffr
- ...Precision Medicine Group is seeking a Senior Clinical Research Associate. You will monitor clinical studies, coordinate activities, and mentor junior staff. The ideal candidate has a university degree in life sciences or health-related fields and at least 3.5 years of...SuggestedRemote workWork from home
$90k - $140k
...A leading clinical research organization is seeking a Clinical Research Associate II or Senior CRA with a focus on Psychiatry or Pain. This remote role involves extensive site monitoring, ensuring adherence to regulations, and engaging in project management activities...SuggestedRemote work$91.5k - $137.3k
...A clinical research organization is seeking a Clinical Research Associate II to oversee study site management in a remote capacity. Ideal candidates will have a degree in a scientific discipline and at least two years of CRA experience, especially in oncology trials. The...SuggestedRemote work$79.72k - $119.58k
...Description The Senior Clinical Research Monitor is responsible for performing ongoing internal reviews of research projects where human subject research is involved to ensure investigators are compliant with federal regulations and guidelines governing clinical research...SuggestedTraineeshipRemote work- ...ICON is looking for a Clinical Research Associate in St. Louis who will play an essential role in clinical trials, ensuring protocol compliance... ...or healthcare-related field and at least 9 months of monitoring experience are essential. ICON values inclusion and offers competitive...Suggested
- ...A leading organization in clinical research is seeking a Clinical Research Associate to ensure that clinical studies are conducted in compliance... ...requirements. The role involves significant travel, monitoring clinical sites, and maintaining robust documentation while supporting...Remote work
$115k - $125k
...A leading clinical research organization is seeking a Clinical Research Associate (CRA) for a remote permanent position based out of CST. The CRA will conduct site monitoring visits, support subject recruitment, and manage communication with study sites. Candidates should...Permanent employmentRemote work$40.55 - $47.2 per hour
...Title: Clinical Research Monitor Location: Upper East Side Org Unit: Genetic Medicine Work Days: Monday-Friday Weekly Hours: 35.00 Exemption Status: Non-Exempt Salary Range: $40.55 - $47.20 *As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role...Work experience placementLocal areaImmediate startMonday to Friday- ...Sr. Clinical Research Associate - South East ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re... ...standards. What You Will Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and...Flexible hours
$91.34k - $114.17k
...A clinical research organization is seeking a Clinical Research Associate in New York City. The position requires a Bachelor’s in Life Sciences or equivalent and 2+ years of monitoring experience, especially in oncology. Responsibilities include ensuring compliance, conducting...- ...WCM-Q in New York is seeking a Clinical Research Monitor to assist with the implementation of quality assurance initiatives. The role includes oversight of investigator compliance with IRB requirements and conducting internal quality audits. The ideal candidate will have...
$40.55 - $47.2 per hour
...Weill Cornell Medical College is seeking a Clinical Research Monitor responsible for overseeing investigator compliance with institutional requirements. This role includes planning and conducting quality audits and providing compliance training. Candidates must hold a...Hourly payMonday to Friday- ...Weill Cornell Medicine - Qatar is looking for a Clinical Research Monitor to assist with compliance initiatives and quality assurance. The role involves oversight of investigator compliance, conducting audits, and maintaining data integrity. The successful candidate will...
- ...Precision Medicine Group is seeking a Manager Global Clinical Monitoring to oversee and develop Clinical Research Associates (CRAs) while ensuring high-quality delivery across clinical projects. This role requires at least 7 years of experience in clinical operations...
- ...Syneos Health is seeking a Senior Clinical Research Associate (CRA) with strong oncology experience located in Town of Belgium, Wisconsin... ...the pharmaceutical industry, managing site qualification and monitoring. Responsibilities include ensuring compliance with regulatory...Remote work
- ...IQVIA in New York is seeking a Clinical Research Associate (CRA) to join our team dedicated to advancing clinical research and improving patient outcomes. In this role, you'll lead site monitoring, ensure compliance with GCP/ICH guidelines, and collaborate with cross-functional...
$30 - $40 per hour
...Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating... ...We are seeking a per diem Assistant Psychedelic Dosing Monitor to support clinical trials focused on psychedelic research for...Hourly payDaily paidReliefFlexible hours3 days per week- ...Parexel International is seeking a Clinical Research Associate (CRA/Sr CRA) to manage oncology studies in the MidWest and West regions of the United States. This role involves site selection, training site staff, and ensuring compliance with ICH-GCP and local regulations...Local area
$70k - $80k
...Responsibilities and Duties Support the LCRA team, in overseeing clinical monitoring operational execution of assigned clinical studies(s).... ...or related healthcare field. Minimum of 1 year of clinical research experience in pharmaceutical, biotechnology, CRO industry. 1...Work at officeLocal areaRemote work3 days per week$240k - $275k
...Job Description Senior Director, Medical Monitor, Hematology-Oncology Location: New York, NY (Hybrid) Department: Clinical Development - Clinical Sciences Reports... ...in pharma/biotech, academic clinical research, or equivalent environment. ~6+ years as...$70k - $80k
Axsome Therapeutics, Inc. is looking for a Clinical Monitoring Associate to support the oversight of clinical studies based in New York City... ...BS in a relevant field and a minimum of one year of clinical research experience. The anticipated salary range is $70,000 - $80,00...- ...ProTrials Research, Inc. is seeking a Contract Senior Clinical Research Associate to oversee clinical trial monitoring and management. This role involves ensuring compliance with protocols and SOPs while managing site personnel training and documentation. The ideal candidate...Contract work
- ...Syneos Health is looking for a Clinical Research Associate II (CRA II) in the United States. This role involves performing site qualification, site initiation, monitoring activities, and ensuring regulatory compliance. The ideal candidate will have a Bachelor's degree...
- ...Health/ inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to perform site management and ensure compliance... ...standards. Responsibilities include site qualification, monitoring, and documentation as well as acting as a liaison with study...Remote workFlexible hours
- ...A leading clinical research organization is seeking a CRA II to manage study sites and ensure compliance with protocols. Responsibilities... ...overseeing patient safety, conducting site visits, and preparing monitoring reports. The ideal candidate will have a minimum of two...Night shift
- ...A leading clinical research organization in New York is looking for a Clinical Research Associate to provide support for clinical trials.... ...assisting with protocol design, site evaluations, and ongoing study monitoring. Candidates should have a BA, BS, RN, BSN or equivalent,...
- ...ABBVIE is seeking a Clinical Research Associate to oversee clinical trials in the NJ/PA area. The role requires engaging with investigative... ...disciplines and at least one year of clinical research monitoring experience. AbbVie offers a competitive compensation package...
$26.77 - $40.05 per hour
...patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists... ...to conduct innovative translational and clinical research that is driving a revolution in... ...Cancer Center: Join the Immune Monitoring Core Facility as a Research Technician!...Monday to Friday- ...Medical Monitor (US Board-Certified Oncologist) 3 days ago Be among the first 25 applicants... ...Description PSI is a leading Contract Research Organization with 30 years in the... ...Monitors provide medical input to global clinical studies and advise the teams and business...Full timeContract workWork from home
- ...Parexel International is seeking a Senior Clinical Research Associate in Idaho to manage and monitor clinical trial sites. This role ensures compliance with regulatory standards and oversees investigator relationships to promote patient safety and study quality. A Bachelor...
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