- 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 ... result, we are seeking a talented and enthusiastic Oncology Clinical Research Nurse to join our exceptional...new clinical trial protocols assigned utilizing Oncore Study - start up task list. + Reviews patient's… more
- Meta (New York, NY)
- …Familiar with software and hardware tooling, electronic data capturing systems that support clinical research studies . 16. Experience in working with ... and/or commercial settings, with a proven understanding of the study lifecycle and clinical research ...research in digital health. 12. Technical expertise in study start -up, human subjects enrollment, consenting, data… 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
- The Mount Sinai Health System (New York, NY)
- …numerous industry-sponsored Phase II and III clinical trials and investigator-initiated studies . The Clinical Research Coordinator II is responsible for ... regulatory and study -specific trainings + Assists with training of new Clinical Research Coordinators + Performs other related duties. **QUALIFICATIONS** +… more
- The 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 (New Brunswick, 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 (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...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
- Actalent (New York, NY)
- …deemed necessary by the site Qualifications: + Minimum of three years in a Study Coordinator or Clinical Research Coordinator role + Oncology experience ... Clinical Research Coordinator *This is a contract position...will act as one of the main CRC's for this study . Please note, as the position and study … 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 ... IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in… more
- Actalent (New Brunswick, NJ)
- …deemed necessary by the site Qualifications: + Minimum of three years in a Study Coordinator or Clinical Research Coordinator role + Oncology experience ... Oncology Clinical Research Coordinator *This is a contract...act as one of the main CRC's for this study . Please note, as the position and study … more
- Actalent (New Brunswick, NJ)
- Oncology Clinical Research Coordinator Job Description: Looking to...act as one of the main CRC's for this study . Please note, as the position and study ... hire a Hybrid full time individual with clinical research experience to act as a...this description. A candidate must help the site and study wherever needed depending on the specific assignment. Responsibilities:… more
- Actalent (New York, NY)
- Clinical Research Coordinator *This is a contract position...will act as one of the main CRC's for this study . Please note, as the position and study ... Description: Looking to hire an onsite full-time individual with clinical research experience to act as a...this description. A candidate must help the site and study wherever needed depending on the specific assignment. Responsibilities:… more
- Actalent (New Brunswick, NJ)
- Job Title: Clinical Research Nurse Job Description As a Clinical Research Nurse, you will play a crucial role in initiating and activating clinical ... and compliance. Hard Skills + 1+ years as a clinical research nurse/OR 2+ years of oncology...years of oncology nursing experience + Experience with Oncore Study - start up task list + Ability to… more
- Actalent (New Brunswick, NJ)
- …current with continuing education and regulatory requirements. Hard Skills + 2-3 years clinical research coordination experience + 1 year oncology required + ... Bachelor's degree in Nursing preferred + Experience with Oncore Study - start up task list + Experience in handling Case Report Forms (CRF) and database queries… more
- The 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
- The 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
- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our ... Vaccination or an approved medical exemption is required to start work. Job Description The Gastrointestinal Oncology Service in...+ Cutting-Edge Research : Contribute to highly productive research programs leading over 25 clinical trials,… more