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Clinical Research Coordinator [CRC} Oncology Clinical Research Unit [CRU] GYNECOLOGY Clinical Research Program [gyn] Position Description, Occupational Summary Provide leadership and coordination in the conduct of multiple, complex oncology clinical trials and research studies including Investigational Products [IP] for the Duke Cancer Institute’s [DCI] Gynecology Clinical Research Program [TNA.
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As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.
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Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.
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Prior experience with clinical research, clinical trials, FDA regulations, and HIPAA considerations is required. Oversee and track invoicing and spending related to clinical research operations.
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Most trials don't require much effort and will be located near you. Potentially get paid to access the most cutting edge medicines combating your disease. Whether you are healthy, or have a specific illness, we'll connect you with the right trial.
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Preform regulatory and safety processes for multiple, complex oncology clinical trials and research studies including Investigational Products [IP] for the Duke Cancer Institute’s [DCI] Melanoma Clinical Research Program [MEL.
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Clinical Trial Support: Lead MSL support of ViiV US sponsored and supported research in specific region, including identifying and selecting appropriate investigators to participate in clinical trials, providing support to Clinical teams and investigators to increase subject enrollment, retention, and site performance.
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Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations such as site and vendor selection, preparing clinical trial budgets.
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This position participates in assessment of the capabilities of affiliate sites to implement clinical research, routinely reviews clinical trials to determine appropriateness for member institutions and assists in the development of strategic research goals for each program.
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IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Conduct site initiation, monitoring, and close-out visits for ophthalmology clinical trials.
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The Associate Director, Statistical Programming will lead the clinical Statistical Programming function with full accountability for SP activities including SDTM, ADaM and statistical outputs; will collaborate with partner functions in Clinical Development Department (e.g., Clinical Operation, Clinical Research, Biometrics) and oversee the vendor SP counterparts.
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Completion of an allied health degree (e.g., Respiratory Therapy, clinical training as a Registered Nurse (RN), Physician's Assistant (PA) or Pharmacist plus four years of healthcare experience; or one of the following equivalents: Radiologic Technology, Licensed Practical Nurse) or Associates degree in Clinical Trials Research related curriculum plus a minimum of six years healthcare experience; or 2.
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Summary: A typical Research Assistant performs a variety of administrative tasks in support of clinical trials and assists in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.
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18+ months Clinical Research Associate (CRA) monitoring experience in clinical research with understanding of clinical trials methodology and terminology. As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge.
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Join Duke Health colleagues at tumor boards, clinical trials research, and have the opportunity to teach Duke Hematology-Oncology fellows in the clinic. This physician partners with community-based and rotating Duke Health Oncologists, an on-site Duke breast surgeon, APPs, Duke Radiation Oncology, on-site specialty pharmacy and has robust clinical services support.
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clinical research trials jobs in Durham, NC
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