- Novo Nordisk (Plainsboro, NJ)
- …of clinical trials improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, IRBs, clinical research vendors). ... identification and mitigation planning for assigned clinical trial sites + Drives and tracks site ...tracks site activation and start-up activities with clinical trial sites to support trial… more
- Abbott (Manhattan, NY)
- …of trends, clinical trial enrollment, and ICH-GCP and clinical research application Adheres to specified site nomination, qualification, and startup ... clinical staff (eg, operations management, study team, Site Contracts Associate ), as needed. **Manage all...needed, provide clinical and technical expertise for clinical trial procedure support + Attend study… more
- Merck (Rahway, NJ)
- …new medicines to patients. The key areas of focus include: (1) diversity in clinical trials, (2) clinical trial recruitment and (3) general education ... wide ( **I** nternal and External) critical communications, focused on our global Clinical Trial efforts. **This role is responsible for supporting the… more
- J&J Family of Companies (Raritan, NJ)
- …will actively participate in or lead aspects of, medical review of clinical trial data, including adverse events, efficacy data, patient screening/eligibility ... Associate Director, Clinical Project Scientist -...Safety Management Plans * Performs medical monitoring/reporting, evaluates ongoing clinical trial data * Liaise with external… more
- Kelly Services (New York, NY)
- …aspects of a clinical trial including, but not limited to, clinical site selection, study visits, preparation of study contracts and budgets, and ... clinical study, including (but not limited to): + Clinical site selection + Site ...plan, case report forms, etc.). + Remain current on clinical trial regulatory requirements and guidelines (eg… more
- Actalent (Basking Ridge, NJ)
- …from monitoring plan + Monitors and updates investigator/ site status for the trial , and supports with clinical trial registry postings + Contributes ... Immediate Opening for Clinical Trials Assistant/ Associate Description: + ...+ Collates data for assessments such as feasibility and site selection and reviews site usability database… more
- Actalent (Paramus, NJ)
- …directly in all study activities, including protocol review, development of study materials, clinical trial site selection and interaction, contractor and ... ON- SITE IN PARAMUS, NJ 5 DAYS/WEEK The Associate Director, Clinical Operations is responsible for...is also a valuable team member providing input into clinical trial implementation, execution, and outcome, building… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …the TMF technical capabilities and oversight of standardization, training, quality, and timely clinical trial documentation across the clinical program. The ... impact. Join Gilead and help create possible, together. **Job Description** The Associate Director, Clinical Records & Information Management will partner with… more
- WuXi AppTec (Cranbury, NJ)
- **Overview** The Clinical Research Associate III Senior Oncology performs and coordinates aspects of field-based and office-based monitoring and data quality ... clinical monitoring and required reporting, including pre-study visits, site invitation visits, routine monitoring visits (both onsite and...or supervisor, including but not limited to mentoring of Clinical Research Associate (CRA) I and II… more
- Astrix Technology (New York, NY)
- …as needed for on- site monitoring visits. + Certification as a Certified Clinical Research Associate / Professional (CCRA / CCRP) or similar credential is ... Clinical Research Associate Clinical ...protocols. + Regionally based and involves working with multiple clinical trial sites across multiple protocols. +… more
- IQVIA (Parsippany, NJ)
- …may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's ...**MINIMUM RECRUITMENT STANDARDS:** + **2.5 years of clinical research coordination experience at site level**… more
- Hackensack Meridian Health (Hackensack, NJ)
- …change. The Clinical Research Nurse is responsible for coordinating and overseeing clinical operations of a clinical trial and participates in assessing, ... complete, up-to-date records on each patient participating in a clinical trial protocol in all applicable systems...Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified … more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …the Clinical Study Lead (CSL) by taking responsibility for areas of clinical trial delivery. This role applies to internally sourced studies and studies ... based in Armonk, NY or Basking Ridge, NJ._ A Clinical Study Associate Manager (CSAM) role supports...maintenance of study systems including but not limited to Clinical Trial Management System (CTMS) and … more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …from monitoring plan + Monitors and updates investigator/ site status for the trial , and supports with clinical trial registry postings + Performs ... to the clinical study team(s) responsible for clinical trial execution. The CSS may be...assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will… more
- Hackensack Meridian Health (Neptune, NJ)
- …works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Responsibilities** + Acts as ... on each protocol and each patient participating in a clinical trial protocol in the clinical...SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified … more
- Bristol Myers Squibb (Berkeley Heights, NJ)
- …the development and implementation of innovative strategies and technologies for clinical trial programming. A ssociate Director develop collaborative ... the development and implementation of innovative strategies and technologies for clinical trial programming + Independently develops, validates, troubleshoots,… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …internally sourced studies and/or CRO/Partnered studies. Collaborates and interacts with clinical trial managers, development program managers, medical monitors, ... orders according to supply plans or as requested by Clinical Trial Management team, to ensure timely...compliant shipment and delivery to investigator sites. Works with Clinical Logistics Associate to complete this activity… more
- Bristol Myers Squibb (New York, NY)
- …and ethical standards + Ensures active participation of FM in providing input on clinical trial site selection and feasibility based on their knowledge ... insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on...in their geography + Ensures FM team's execution of clinical trial support activities (as per established… more
- Bristol Myers Squibb (Madison, NJ)
- …aligned medical communications plans; adjust communications plans in accordance with clinical trial results/milestones and changes in the healthcare landscape ... Professional (CMPP), and ISMPP active member highly desired + Understanding of clinical trial design and execution, statistical methods and clinical… more
- Merck (Rahway, NJ)
- …chains. This role works closely with internal stakeholders in the GCS (Global Clinical Supply), GCTO (Global Clinical Trial Organization), procurement, and ... and influence stakeholders and suppliers in the context of a challenging clinical trial environment. + Interpersonal and communication skills. Formal… more