Clinical Research Monitor
$40.55 - $47.2 per hourWeill Cornell Medicine
Overview 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 when Hired for NYC Offices 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 the WCM, including the 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. To Apply To apply, visit #J-18808-Ljbffr Weill Cornell Medicine
$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$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...SuggestedPermanent employmentRemote 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- ...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...SuggestedRemote work
- ...Precision Medicine Group is seeking a remote Clinical Research Associate II based in Texas or California. The ideal candidate will manage... ...and data integrity. Responsibilities include site management, monitoring, and compliance with audit standards. The position requires...SuggestedRemote work
$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...Remote work- ...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...Remote workWork from home
- ...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
- ...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
$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...$150k - $170k
...sounds like you, keep reading! Role Summary We are seeking a Clinical Monitoring Manager to oversee in‑house Oversight CRAs that will manage... ...gastrointestinal clinical trials is a plus. Certification as a Clinical Research Associate (CCRA) or equivalent preferred. Experience with...Interim roleWork at office- 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...
- ...Senior Clinical Research Monitor 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...Remote jobFull timeTraineeshipWork at officeLocal areaShift work
$70k - $80k
...information, visit and follow us on LinkedIn and X . About This Role Axsome Therapeutics is seeking a Clinical Monitoring Associate (CMA). Supporting the Lead Clinical Research Associate (LCRA), the CMA provides administrative and operational support to assist effective...Work at officeLocal areaRemote work3 days per week- ...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...
- ...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
$70k - $80k
Axsome Therapeutics, Inc. in New York City is seeking a Clinical Monitoring Associate to support the Lead Clinical Research Associate in managing clinical studies. This position involves overseeing monitoring processes and ensuring compliance throughout the clinical trial...3 days per week- ...ICON Strategic Solutions is looking for a Clinical Research Associate who will lead clinical trial monitoring with a focus on quality and continuous improvement. The individual will ensure adherence to protocols and conduct site visits to support successful trial execution...
- ...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
- ...Medical Device company, has engaged GForce Life Sciences to source a skilled Clinical Site Lead (CSL). The CSL will oversee clinical study site maintenance, data collection, and field monitoring to ensure compliance with protocols, regulations, and Good Clinical...Local areaRemote workWork from home
- ICON Strategic Solutions is seeking a Sr. Clinical Research Associate to lead clinical trial monitoring tasks in North East United States. The role requires a Bachelor's degree in a relevant field and extensive experience as a Clinical Research Associate. Candidates should...
- 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...
- Weill Cornell Medicine is seeking a Clinical Research Monitor to ensure compliance with institutional and federal regulations. The role involves overseeing audits, assisting with training, and managing data operations. The ideal candidate will have a Bachelor's degree and...
- ICON in Pennsylvania is seeking a Sr. Clinical Research Associate to lead clinical trial monitoring and ensure compliance with protocols and regulations. The ideal candidate will have a Bachelor's degree and extensive experience in clinical trials. Responsibilities include...
- Job Description Job Description Duties: Demonstrates competency with rhythm strip interpretation. Immediately notifies RN and/or physician of any life threatening arrythmias. Notifies RN of changes in patient rhythm. Demonstrates competency in activating...Immediate startShift work
- ...Senior Medical Director, Clinical Development (Medical Monitoring) About the Company Rapidly growing organization in the oncology & hematology industry... ...clinical medicine and practical experience in medical research or clinical development. A minimum of 10-15 years' of...
- A healthcare organization is seeking a Clinical Research Program Manager to oversee quality assurance for clinical trials. The candidate will... ...compliance with regulatory standards and manage ongoing monitoring activities. Required qualifications include a Bachelor's degree...
- Job Description Job Description BronxWorks helps individuals and families improve their economic and social well-being. From toddlers to seniors, we feed, shelter, teach, and support our neighbors to build a stronger community. In all aspects of our work, we strive...Permanent employmentWork at officeLocal areaAll shiftsShift work
- ...Job Description Job Description PRIMARY FUNCTION/PURPOSE: The Safety Monitor will be directly responsible for monitoring all activities in the physical location and ensuring civility amongst residents, visitors, and staff. This individual controls access to the...Shift work
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