- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and immune disorders. **Summary** This position supports the strategy for driving global Clinical Study Start -Up activities for PV Safety Operations. This ... study safety reporting and activities. + Global Clinical Study Start -Up Documentation: Reviews... protocols to ensure consistency in safety requirements across studies related to a similar compound. Develops and maintains… more
- System One (Basking Ridge, NJ)
- …from Basking Ridge, NJ. JOB DECRIPTION: Assist in planning and execution of clinical studies , under the supervision of the Study Manager role the Study ... Role: Clinical Study Associate I Type: 12...attention. Skills: Demonstrates knowledge of complex processes related to clinical studies , regulatory issues, CRO operations, and… more
- Vitalief (New Brunswick, NJ)
- …can work one day per week remotely. Responsibilities: + Under the direction of the Clinical Research Study Site Leader, this resource will be responsible for ... we are seeking a talented and enthusiastic Oncology Pediatrics Clinical Research Nurse to join our exceptional...new clinical trial protocols assigned utilizing Oncore Study - start up task list. + Reviews patient's… more
- Vitalief (New Brunswick, NJ)
- …departments as needed. + Facilitates clinical trial billing administrative start -up, insuring clinical research billing and regulatory compliance. ... beginning of protocol submission to the end of the study utilizing OnCore CTMS system. + Performs regular audits... of financial data and transactions. + Experience in clinical research administration; knowledge of regulatory, financial… more
- Mount Sinai Health System (New York, NY)
- …to assist in the daily activities of clinical research studies , including collection and organization of study information. Assists in preparing grant ... Advancing medicine. Healing made personal._** **_Roles & Responsibilities:_** The ** Clinical Research Coordinator (CRC)** at the **Alzheimer's...at Icahn School of Medicine at Mount Sinai, assists clinical studies sponsored by the NIH and… more
- HSS (New York, NY)
- …Previously worked with industry sponsored/funded studies (specifically independent execution of study start up to close out) + Previous management experience ... can be part of our transformation across the enterprise. Clinical Research Manager - Industry Full-Time Summary:...will be responsible for submitting all visits required for study milestones (eg start -up/initiation, quality & audit… more
- Actalent (Edison, NJ)
- …professional development. Hard Skills + 2-3 years of experience as a clinical research coordinator + Experience with Oncore Study - start up task list + ... Job Title: Clinical Trial Specialist Job Description As a ...trial protocols. This includes the preparation and review of study tools, verification of approvals, and collaboration with the… more
- IQVIA (Parsippany, NJ)
- …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... study documentation. * Act as a mentor for clinical staff including conducting co-monitoring and training visits. *...leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences… more
- IQVIA (Linden, NJ)
- …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice (GCP) and ... management work to ensure that sites are conducting the study (ies) and reporting study data as required...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- IQVIA (Parsippany, NJ)
- …prior monitoring experience. * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice ... management work to ensure that sites are conducting the study (ies) and reporting study data as required...leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences… more
- Vitalief (New Brunswick, NJ)
- …is 100% on-site in New Brunswick, NJ Responsibilities: + Under the direction of the Clinical Research Study Site Leader, this resource will be responsible ... new clinical trial protocols assigned utilizing Oncore Study - start up task list. + Collaborate with...start up task list. + Collaborate with the clinical research team to ensure timely prescreening… more
- IQVIA (New York, NY)
- IQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring experience in one of the following therapeutic areas: Central Nervous ... including on-site monitoring. \#CRAFSAJD IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Parsippany, NJ)
- **Job Overview** Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- Pfizer (New York, NY)
- …and execution of clinical studies and delivering on innovative clinical study designs, high quality trial execution, safety assessment and interpretation ... is to lead and coordinate the development of multiple studies for novel biological and small molecule therapies for...and remit of OESD is represented as need within clinical study teams (eg Research … more
- Mount Sinai Health System (New York, NY)
- …funding limitations; * Assist in training staff and conduct of activities related to clinical research studies including tasks such as obtaining screening ... clinical trials: * Maintain operational management of clinical research protocols. * Oversees and manages...research processes and procedures. * Develop SOPs for study start -up, procedures, close-out, and other policies… more
- IQVIA (Bridgewater, NJ)
- …working flexibly? If so, come and join us - IQVIA are looking Clinical Research Assistant. This role has an **immediate start working 16-20 hours a week** ... Are you looking for an opportunity in Clinical Research ? Do you want to...to day responsibilities will include:** + Verifying and/or correcting research study information on source documents; researching… more
- Terumo Medical Corporation (Somerset, NJ)
- …of final study reports. Clinical operational activities: + Support trial study start -up phases (support in writing study protocol, identification of ... clinical trial support to sites/investigators that are participating in the clinical research and participate in investigator launch meetings. Regulatory… more
- Mount Sinai Health System (New York, NY)
- … program. + Liaison with industry sponsors and CROs. Clinical Research Responsibilities: + Responsible for coordinating study enrollment, establishing a ... process, cancer treatment modalities, and the process of conducting clinical research . The candidate will follow a...the protocol; and monitors test results, as appropriate Documents clinical study and therapy in patient's chart… more
- Vitalief (New Brunswick, NJ)
- …of complex environments with multiple stakeholders and competing priorities. + Understanding of clinical trial processes from study start -up through study ... and Learning & Development Solutions addressing the Human Capital epidemic in the Clinical Research Industry and supporting our clients in planning and execution… more
- The Cigna Group (Morris Plains, NJ)
- … research alongside innovative and thought-provoking reports. Through our research , we support clinical and business decision-making enabling the ... and gain exposure to a breadth of expertise in clinical , research , payer and provider solutions teams...depending on relevant factors, including major and year of study . If you will be working at home occasionally… more