- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …CRA experience preferred.Time spent directly in a medical environment (eg as a Study Site Coordinator ) is also considered relevant. preferred TravelAbility ... review spreadsheet.Compile and maintain CRO Oversight Monitoring (CROOM) visit output.Analyze study site metrics reports to identify potential areas of… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …experience preferred.Time spent directly in a medical environment (eg as a Study Site Coordinator ) preferred.Familiarity to a Japan-based organization ... be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence...identification activities in collaboration with the CRO and the study team. Oversee the site qualification process.Monitor… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …experience required. Time spent directly in a medical environment (eg as a Study Site Coordinator ) is also considered relevant. preferred Familiarity ... site identification activities in collaboration with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... elements of the quality management system are in place for studies conducted in partnership with non-commercial organizations (eg Non-Governmental Organization… more
- Danaher Corporation (New York, NY)
- …the following position in our office in remotely based in the USA Study site and study coordinator Come join a fantastic team! YOUR RESPONSIBILITIES + ... incl. coordinating equipment preparation, shipment, installation, de-installation and handling on- site during the course of the study ...handling on- site during the course of the study + Support training of the study … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …CRA experience preferred. + Time spent directly in a medical environment (eg as a Study Site Coordinator ) is also considered relevant. preferred **Travel** + ... disorders. **Summary** Assist in planning and execution of clinical studies , under the supervision of the Study ...maintain CRO Oversight Monitoring (CROOM) visit output. + Analyze study site metrics reports to identify potential… more
- The Mount Sinai Health System (New York, NY)
- …competent workforce to work with diverse populations. Serves as Clinical Research Coordinator of multi- site clinical study activities (activation, ... The Clinical Research Coordinator position is located in the lab of...a liaison among the Principal Investigator/research team, participating sites, study sponsors, and other collaborators to administer protocols, ensuring… more
- Actalent (Newark, NJ)
- Study Coordinator *This is a contract position...listed in this description. A candidate must help the site and study wherever needed depending on the ... Source documents + Specimen collection and processing + Any study efforts deemed necessary by the site ... Qualifications: + Minimum of five years in a Study Coordinator or Clinical Research Coordinator… more
- Actalent (Newark, NJ)
- …patient follow-up and pre-screening. This individual will be responsible for full study coordinator duties. Duties and Responsibilities: * Chart review of ... clinical research background to act as the Clinical Research Coordinator for a research site in Newark,...data entry * Scheduling patient appointments for their in-person study visit * Consenting patients Skills: Data entry, Ophthalmology,… more
- Atlantic Health System (Morristown, NJ)
- …in team problem-solving methods. + Additional duties as assigned by physician, site coordinator or practice manager + Protect operations by maintaining ... in team problem-solving methods. + Additional duties as assigned by physician, site coordinator or practice manager. + Maintains a cooperative relationship… more
- Hackensack Meridian Health (Nutley, NJ)
- …outlining standard of care and research costs. Finalizes budget draft with budget coordinator . + Reviews proposed study protocols to evaluate factors such as ... and serve as a leader of positive change. The **Clinical Research Coordinator ** is responsible for coordinating and overseeing clinical operations of all assigned… more
- Hackensack Meridian Health (Neptune, NJ)
- …meetings, and conferences/in-service education sessions as required. Including but not limited to study Site Initiation Visits and Study Close Out Visits. ... a leader of positive change. The **Senior Clinical Data Coordinator ** is responsible for the oversight of the data...while maintaining data integrity for all assigned clinical research studies . **Responsibilities** A day in the life of a… more
- Hackensack Meridian Health (Hackensack, NJ)
- …meetings, and conferences/in-service education sessions as required. Including but not limited to study Site Initiation Visits and Study Close Out Visits. ... as a leader of positive change. The **Clinical Data Coordinator ** is responsible for data entry and query management,...while maintaining data integrity for all assigned clinical research studies . **Responsibilities** A day in the life of a… more
- RWJBarnabas Health (Mountainside, NJ)
- Research Coordinator Physiatry - Full Time - Hybrid - Mountainside, NJReq #:45926 Category:Research Status:Full-Time Shift:Day Facility:Childrens Specialized Hosp ... We are seeking a highly motivated and skilled Research Coordinator to join our team. Under the direction of...will be involved in overseeing experiments and clinical research studies at the physiatry section at Children s Specialized… more
- HSS (New York, NY)
- …may evolve as studies progress. The applicant must be available on site at the main hospital. Clinical and Regulatory responsibilities: + Conducts the informed ... too can be part of our transformation across the enterprise Clinical Research Coordinator - Knee Service Full-Time Overview: Clinical Research Coordinator will… more
- Hackensack Meridian Health (Edison, NJ)
- …healthcare and serve as a leader of positive change. The Research Nurse Coordinator is responsible for ensuring that the clinical research is conducted according to ... changes within the protocol. + Facilitates all audits of study with staff of JFK Medical Center, sponsor, FDA,...Center, sponsor, FDA, and other regulatory agencies. + Reviews studies for feasibility and for competing protocols prior to… more
- Hackensack Meridian Health (Totowa, NJ)
- …healthcare and serve as a leader ofpositive change. The Research Nurse Coordinator is responsible for ensuring that the clinical research is conducted according ... A day in the life of a Research Nurse Coordinator at Hackensack Meridian Health may include: + Assists...changes within the protocol + Facilitates all audits of study with staff of Hackensack University Medical Center, sponsor,… more
- Vitalief (New Brunswick, NJ)
- …in site preparation for trials including protocol feasibility, preliminary study budget, startup meeting preparation, training staff, and preparation of IRB ... annually Work Location: Work is 5 days per week on- site in New Brunswick, NJ. Ability to work one...applications and preparation of regulatory documents, study documents and forms. + Conducts trial visits by… more
- Weill Cornell Medical College (New York, NY)
- …guidelines for the collection of clinical data and or administration of clinical studies . + Ensures compliance of general and study specific regulatory related ... routine monitoring and closeout visits. + Works closely with sponsor, site and study personnel on relevant regulatory issues. Develops policies and procedures… more
- New York University (New York, NY)
- Drs. Shabnam Javdani and Erin Godfrey are seeking a project coordinator to provide full-time intervention support on Systems Aligning for Equity (SAFE) Spaces, a ... supporting staff. The primary goal of the Counseling and Coaching Assistant Project Coordinator will be to provide direct services counseling and coaching to staff… more