IP Dispensing Clinical Research Coordinator I — Compliance
Dm Clinical Research Group
DM Clinical Research Group in Philadelphia, PA is seeking an Unblinded Clinical Research Coordinator I to join our clinical trials team. The role involves dispensing Investigational Products (IP) and ensuring IP accountability within protocol guidelines. You will manage IP stock, assist in site startup activities, train new staff, and ensure regulatory documents are current. Strong communication, organization, and multitasking are essential, with a preference for bilingual Spanish speakers. #J-18808-Ljbffr Dm Clinical Research Group
- A clinical research organization in New Jersey is seeking a Registered Nurse... ...Unblinded Clinical Research Coordinator role. Responsibilities include compounding and dispensing investigational products as... ...research trials, ensuring compliance, and maintaining medication...Suggested
- DM Clinical Research is seeking an Unblinded Clinical Research Coordinator II responsible for dispensing Investigational Products (IP) and managing IP accountability. You will support startup activities, ensure regulatory readiness, and supervise medication records for...Suggested
$27 - $32 per hour
...Clinical Research Coordinator I Boston, Massachusetts, United States Join Us... ...investigational product (IP) accountability for assigned... ...receipt, storage, dispensing, reconciliation, temperature... ...under supervision, ensuring compliance with protocol and site SOPs...SuggestedHourly payFlexible hours$32 - $37 per hour
...Shaping the Future of Clinical Research Adams Clinical is... ...the Clinical Research Coordinator II role at our Bronx... ...investigational product (IP) accountability for... ...receipt, storage, dispensing, reconciliation, temperature... ...disposal, ensuring compliance with protocol,...SuggestedHourly payFlexible hours$70.48k - $74.79k
...medical education, scientific research, and direct patient care.... ...to join our team as a Clinical Research Coordinator. The Oncology Clinical... ...patient safety, overall compliance in the conduct of the study... ...Pharmacy to ensure timely dispensation of IP per CTO processes/...SuggestedWork at office$35 - $42 per hour
...Job Description Job Description Job Title: Clinical Research Coordinator Job Description The Clinical Research Coordinator supports oncology... ...processing, to ensure high-quality research conduct and compliance with regulatory and institutional requirements....Contract workTemporary workWork at office- ...Philadelphia, PA 19107DM Clinical Research is looking to hire an... ...Unblinded Clinical Research Coordinator I to join our team.... ...be responsible for dispensing Investigational Products (IP) as part of clinical research... ...all medications Ensure compliance with study-specific...
- ...Cornell Medicine - Qatar is seeking a clinical research professional to monitor data management... ...aspects of trial operations. The role coordinates special research projects, prepares... ...sponsor sites and study personnel to ensure compliance with #J-18808-Ljbffr Weill Cornell...
$56.2k - $81.5k
...Medicine is seeking a highly motivated and detail-oriented Clinical Research Coordinator (CRC) to support a diverse portfolio of oncology research... ...projects, ensuring that all studies are conducted in compliance with institutional policies, Good Clinical Practice (GCP)...Full timeWork experience placementWork at officeRemote work- The Mount Sinai Health System is seeking a Clinical Research Coordinator to assist in daily study activities, obtain informed consent, and organize... ...You will help prepare grant-related documents and ensure compliance with IRB requirements. This role requires a Bachelor's or...
- Mount Sinai Morningside in New York seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent... ...and IRB submissions, and help ensure regulatory compliance. The role involves coordinating participant screening, data...
- ...University Irving Medical Center in New York seeks a full-time Clinical Research Coordinator to support obesity and cardiometabolic studies. Reporting... ..., you will coordinate study activities, ensure protocol compliance, and contribute to data collection and analysis....Full time
- Position: Unblinded Clinical Research Coordinator II Location: New York City, NY Job Id: 1... ...individual will be responsible for dispensing Investigational Products (IP) as part of clinical research... ...of all medications Ensure compliance with study-specific blinding plans...
- Mount Sinai Health System seeks a Clinical Research Coordinator II to oversee the operational delivery of cellular therapy trials, ensuring protocol... ...protocol execution, data collection, and regulatory compliance in a high-stakes setting. The role requires 2 years of clinical...
$20 - $29.08 per hour
...comSummarized Purpose: Study coordinator to support ongoing large clinical study in US. Completes... .... Interacts with the research site team and other interdepartmental... ...required, may complete IP accountability logs and... ...* Reports suspected non-compliance to relevant site staff. *...Local area- Mount Sinai Morningside is seeking a clinical research professional to generate and interpret highly complex data, develop... ...tasks while ensuring regulatory and protocol compliance across sites. The role involves coordinating with investigators and regulatory teams,...
- ...Health System in New York, NY seeks a clinical research professional to generate, reconcile and... ...training, mentor staff, and ensure compliance across study procedures. The role involves... ...spanning protocol submissions, site coordination and regulatory tasks. A strong background...
- Experienced Clinical Project Manager - Inflammation (Sponsor Dedicated... ...Draft, review, and coordinate key study documents including... ...experience within clinical research Experience running clinical... ...The Company is committed to compliance with the Americans with Disabilities...Remote jobContract workInterim roleImmediate startFlexible hoursShift work
$35 - $38 per hour
...Job Description Job Description Senior Clinical Research Coordinator *Great opportunity to work on cutting edge oncology clinical trials... ...clinical trial protocols, ensures regulatory and ethical compliance, and maintains accurate research documentation throughout...Contract workTemporary work- ...We are seeking a Senior Clinical Research Coordinator to lead the day-to-day execution... ...source documentation in compliance with ICH-GCP, FDA... ...submission. · Manage IP (investigational product)... ...including receipt, storage, dispensing, and reconciliation per protocol...
- ...Clinical Trial Manager - Full Service Syneos Health is a leading... ...safety, protocol/GCP/regulatory compliance and data integrity. Oversees... ...and Data Management to coordinate delivery handoffs and meet expected... ...conduct of a clinical research project. Demonstrates critical...Contract workRemote workFlexible hours
- DescriptionThe Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed...Hourly payTraineeshipWork at officeLocal area
$105k - $157.49k
DescriptionWe are seeking a Clinical Trials and Regulatory Affairs... ...Psychotherapy and Trauma Research (the Center) at the Icahn School... ...Committee) • Ensure compliance with GCP, and regulatory guidelines... ...• Supervise research coordinators on all aspects of regulatory...TraineeshipLocal area- DescriptionWe have an immediate opening for a Clinical Research Coordinator who will work with human specimens. The Clinical Research Coordinator is an entry research position, responsible for assisting in clinical research studies, obtaining informed consent, collecting...Hourly payTraineeshipWork at officeLocal areaImmediate start
- DescriptionThe Parsons Research Center for Psychedelic Healing (PRCPH) and the Division of Traumatic Stress Studies, joint... ...Medical Center (JJP VAMC), have an opening for a full-time clinical research coordinator to oversee day-to-day operations of research studies....Hourly payFull timeTraineeshipLocal areaRemote work
- Syneos Health is seeking a Clinical Trial Manager to oversee site management, clinical monitoring, and central monitoring with... ...focus on patient safety, data integrity, and regulatory compliance. You will coordinate cross-functional teams, manage budgets, and ensure study...Remote job
- Syneos Health in United States, Pennsylvania seeks an experienced Clinical Trial Manager to lead site management and monitoring... ...oversight, and adherence to GCP and regulatory standards. You will coordinate with CRAs, data management, and start-up teams to ensure on-time...
- ...United States (Georgia), is seeking a Clinical Trial Manager for Full Service operations... ...ensuring patient safety and regulatory compliance across studies from activation to... ...lead CRAs and cross-functional teams, coordinate with data management, start-up, and recruitment...
$120k - $135k
Clinical Project Manager - Oncology (Client Dedicated/Remote) Updated... ...about advancing cancer research and bringing innovative therapies... ..., and specialty providers Coordinate Clinical Trial Team (CTT)... ...Ensure inspection readiness and compliance with applicable regulations...Remote jobContract workWork at officeImmediate startWorldwideFlexible hours- ...Clinical Research Coordinator I Columbia University Irving Medical Center (CUIMC) provides global leadership in scientific research, health... .../or communication between the Principal Investigator and compliance offices and study sponsors. Maintain accurate and complete...Work at officeLocal areaFlexible hours
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