See more Collapse

Clinical Trials Manager

2 months ago


Wilmington, United States Nemours Full time

The **Clinical Trials Manager**-Mosely Institute provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities of research nurses and staff conducting studies and oversees the management of all clinical research projects conducted at Nemours Children's Hospital
- Delaware. Managing both Hematology and Oncology Research Associates, this position will support the Moseley Institute in Delaware Valley. Collaborating with Research partners across multiple Nemours sites and Non-Nemours sites this leadership role will work in conjunction with the enterprise coalition for the Nemours Center for Cancer and Blood Disorders (NCCBD).
**Essential Functions**:
Strategic Planning and Development:
1. Meet with the medical staff and faculty on a regular basis to assess their needs pertaining to clinical trials research.
2. Develop goals and performance measures in conjunction with the medical faculty to ensure growth and development of the clinical trials program.
3. Meet regularly with the Associate Administrator - Delaware to provide feedback on new initiatives, performance of on-going initiatives, and seek feedback for future programmatic development.
4. Assist with budget management of the clinical trials program in Delaware Valley

Supervision and Oversight:
1. Supervise and coordinate the daily activities of the research coordinators and staff.
2. Provide guidance and oversight for submissions to scientific and ethical review committees.
3. Review new research protocols and ensure there is adequate and appropriate staffing for current and planned protocols.
4. Conduct interviews and make hiring recommendations.
5. Provide oversight, periodic review including rounding, and feedback to clinical trials staff.
6. Provide procedures for systematic record keeping, drug accountability, patient interactions, equipment tracking, and good clinical practices.
7. Provide pre-review prior to external audit or investigations.
8. Responsible for performance management of designated staff.

**Qualifications**:

- Five years of Clinical Research Coordinator experience or equivalent experience required, with a minimum of 5 years clinical pediatric experience.
- Masters degree preferred; bachelors degree with appropriate experience may be acceptable.
- BSN with active Delaware Nursing License preferred


We have other current jobs related to this field that you can find below


  • Wilmington, United States Nemours Children's Health Full time

    Job Description The Clinical Trials Manager-Moseley Institute provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities of research nurses and staff conducting studies and oversees the management of all clinical research projects conducted at...


  • Wilmington, United States Nemours Full time

    The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities of clinical research assistants, clinical research coordinators, clinical research nurses and staff conducting studies and oversees the management of all...


  • Wilmington, North Carolina, United States Novartis Farmac??utica Full time

    Clinical Development Medical Director – Immunology, Rheumatology Job ID: REQ–Date: Jul 09, 2024Location: USA Summary As the Clinical Development Medical Director (CDMD) Immunology, you will lead clinical teams dedicated to autoimmune rheumatic disease development programs in indications of lupus, including both systemic lupus erythematosus and lupus...


  • Wilmington, United States Nemours Full time

    The Lead Clinical Research Nurse will provide technical guidance and subject matter expertise to facilitate the coordination and conduct of clinical research studies and/or clinical trials within the department/division/unit within Nemours. This individual will play a key role by helping to coordinate, implement and complete clinical research studies and/or...


  • Wilmington, North Carolina, United States Novartis Farmac??utica Full time

    Onsite Location: East Hanover, New Jersey Hybrid About the role: Novartis is deeply committed to transforming the lives of people living with solid tumors, blood cancers and serious or life–threatening blood disorders. We believe that anyone living with these conditions has the right to a life free from pain, free from symptoms and free from disease –...


  • Wilmington, North Carolina, United States Novartis Farmac??utica Full time

    (Senior) Clinical Development Medical Director – Rheumatology Job ID: 381169BRDate: May 20, 2024Location: USA Summary As a Clinical Development Medical Director in our Immunology Development Unit, you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. The Clinical...


  • Wilmington, North Carolina, United States Novartis Farmac??utica Full time

    Clinical Development Director (CDD) – Cardio, Renal, Metabolism Job ID: REQ–Date: May 21, 2024Location: USA Summary The Clinical Development Director (CDD) in the Cardio Renal & Metabolic (CRM) Development Unit is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end–to–end clinical development...


  • Wilmington, United States Nemours Children's Health Full time

    Job Description The Clinical Research Coordination Lead will provide technical guidance and subject matter expertise to facilitate the coordination and conduct of clinical research studies and/or clinical trials within the department/division /unit within Nemours. This individual will play a key role by helping to coordinate, implement and complete clinical...


  • Wilmington, North Carolina, United States Novartis Farmac??utica Full time

    Senior Clinical Development Medical Director, Oncology Job ID: 393918BRAug 02, 2024Location: East Hanover, New Jersey (Hybrid) Summary Novartis is deeply committed to transforming the lives of people living with solid tumors, blood cancers, and serious or life–threatening blood disorders. We believe that anyone living with these conditions has the right to...


  • Wilmington, North Carolina, United States Novartis Farmac??utica Full time

    Senior Clinical Development Medical Director – Cardio Renal Metabolism Job ID: REQ–Jul 01, 2024USA Summary The Senior Clinical Development Medical Director (Sr. CDMD) is the clinical leader of a section of a clinical program (e.g., an indication, a new formulation, or a specific development phase), or a large, complex trial, under the leadership of the...

  • Biostatistician I

    4 weeks ago


    Wilmington, United States Catalyst Clinical Research LLC Full time

    Job DescriptionJob DescriptionPosition Summary:  As a Biostatistician I you will be a key member of the Development Operations, Biostatistics Team. You will plan, analyze, and summarize the results of individual clinical studies or groups of studies (integrated summaries) and assist in coordination of the development and review of regulatory submissions...

  • Biostatistician I

    4 weeks ago


    Wilmington, United States Catalyst Clinical Research LLC Full time

    Job DescriptionJob DescriptionPosition Summary:  As a Biostatistician I you will be a key member of the Development Operations, Biostatistics Team. You will plan, analyze, and summarize the results of individual clinical studies or groups of studies (integrated summaries) and assist in coordination of the development and review of regulatory submissions...


  • Wilmington, United States Fladger Assoc. Inc. Full time

    Job DescriptionJob DescriptionWilmington, DEContract Duration: 12-36 monthsRate: NegotiableResponsibilities:Excellent employment opportunity for a Specialist Study Management in the Wilmington, DE area. Candidates must be local to Wilmington, DE, non-remote position Own and maintain quality for the study file as the local study team TMF ownerResponsible for...


  • Wilmington, United States Fladger Assoc. Inc. Full time

    Job DescriptionJob DescriptionWilmington, DEContract Duration: 12-36 monthsRate: NegotiableResponsibilities:Excellent employment opportunity for a Specialist Study Management in the Wilmington, DE area. Candidates must be local to Wilmington, DE, non-remote position Own and maintain quality for the study file as the local study team TMF ownerResponsible for...


  • Wilmington, United States Nemours Children's Health Full time

    Job Description Clinical Research Coordinator inOncologysupporting the Mosley Institute/NCCBD (Nemours Center for Cancer & Blood Disorders) - coordinates, implements and completes clinical research studies and/or clinical trials by assisting in screening oncology patients, obtaining parental permission/assent/consent forms, educating parents/participants,...


  • Wilmington, Delaware, United States Nemours Full time

    The Clinical Research Coordinator coordinates, implements and completes clinical research studies and/or clinical trials by assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and conducting study...


  • Wilmington, United States Masis Professional Group Full time

    Medical Affairs Manager, US (Oncology, Endocrinology, Radiopharmaceuticals)*Candidate MUST live a within a commutable distance to Wilmington, MA. Hybrid is a must.Company Overview:Join a small but groundbreaking radiopharmaceutical development organization that retains its start-up spirit and is deeply committed to advancing patient care and developing new...


  • Wilmington, United States AstraZeneca Full time

    At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you are our kind of person.A position providing...


  • Wilmington, United States Nemours Full time

    The primary function of the Administrative and Data Coordinator is to provide administrative, secretarial, and technical support to the Clinical Trials Manager and the Clinical Research Core on a daily basis. Job duties include but are not limited to: Patient scheduling, registration and Greenphire management. Work in concert with other members of the...


  • Wilmington, Delaware, United States Nemours Full time

    The primary function of the Administrative and Data Coordinator is to provide administrative, secretarial, and technical support to the Clinical Trials Manager and the Clinical Research Core on a daily basis. Job duties include but are not limited to: Patient scheduling, registration and Greenphire management. Work in concert with other members of the...