of the Sylvester Comprehensive Cancer Center Clinical Trials portfolio in the study of Sarcoma cancers. Duties... Career worklet, please review this . Job Summary: This faculty position will have clinical, research and administrative...
of underlying clinical study design. Provides administrative support and meeting coordination for clinical trials in scheduling... support, and study training. Sets-up, updates and maintains clinical trial-related trackers such as regulatory documents...
with experience and qualifications. Required Qualifications D.O. Field of Study: OMM or related field (degree must be conferred... on or before agreed upon start date) Certifications, Registrations, and/or Licenses: D.O. Field of Study: OMM or related field...
(for an indication or for multiple studies within an indication) from study start up through to regulatory submission. In collaboration... with cross-functional teams, external partners, and support Data Managers, may serve as the lead study data manager for a large...
Additional Information: Shift 8-4 Hours 40hrs/week Prepare labels and label clinical study samples. Assist... in collection of clinical study samples or necropsy. Aliquot clinical study samples. (serum, swab effluents, fecal samples, animal...
+ years’ experience in pharmaceutical industry and/or clinical research organization, including 7+ years clinical study... partners and other vendors. Represent Clinical Operations at the Global Program Team (GPT) and partner with Global Clinical...
Pay rate range: $25.00 - $26.78/hr Shift 8-4, Hours 40hrs/week Duties: Prepare labels and label clinical study... samples. Assist in collection of clinical study samples or necropsy. Aliquot clinical study samples. (serum, swab effluents...
CQA team and provides oversight for and participates in, auditing services in support of Alkermes Clinical Programs... by conducting clinical site, vendor qualification, internal systems and document audits to ensure compliance with cGCPs. The CQA...
regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the... of applicable clinical research regulatory requirements. You should have: A Bachelor's degree in a health care...
clinical development paradigm, especially around clinical study operations and have global or regional experience. Has 5... will have strategic responsibility for a global Start-up Solution Unit Lead focused on Clinical Site Agreements (CSA). You operate...
); partnering with Clinical Operations on study deliverables Ensure CRF design supports data collection in alignment with the... of the Clinical Study Reports Interact with key stakeholders across Clinical Development functional areas Role requires...
teams to support all phases of a clinical study including protocol, CRF, and monitoring plan development, essential document... will provide leadership, oversight and operational direction to a team of in-house and regional Clinical Research Associates (CRAs...
improvements Review clinical protocols for operational feasibility and anticipate potential study delivery challenges Draft... and maintain clinical project timelines; proactively escalate risks to the Study Lead Support clinical trial budget analysis...
) desirable. Proven experience in all aspects of clinical study planning and startup (including budget and resource planning... clinical trial strategy while accountable for successful project execution and delivery of clinical operational budget...
Job Overview: Perform monitoring and site management work to ensure that sites are conducting the study(ies...) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements...
, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department... devices and supplies to clinical sites. Perform study device accountability and reconciliation. Assist senior staff...
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies...) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements...
clinical trial(s) from start up through study close out in accordance with the study protocol, GCP, and Velocity’s SOPs.... Responsibilities: Role & Responsibilities: Serve as leader of a study team to execute clinical trials Mentor and train staff...
/Responsibilities: Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs... risk and improve quality in the conduct of a clinical research study Develop, coordinate, and implement research...
school diploma or equivalent required; Associate or Bachelor’s preferred · Current Good Clinical Practice (GCP...Pay: Up to $27.00 per hour Job title: Clinical Research Coordinator (CRC) with Regulatory Specialist Expertise...