Provide critical scientific support across clinical and translational research projects in endocrinology, diabetes, and liver disease.
Compensation
$61,000 - $72,000; Commensurate with education and experience.
Responsibilities
Coordinate and implement research activities across multidisciplinary collaborators and multiple clinical research studies
Manage process for participant research visits and ensure completion of required study procedures, assessments, laboratory testing, and follow-up activities
Lead informed consent activities and communicate research procedures to study participants
Perform liver imaging using transient elastography
Identify and resolve issues affecting study implementation and participant follow-up
Requirements
Bachelor’s degree in biology or a related field
Master’s degree in biology or a related field
Doctoral degree in biology or a related field
Nice to have: clinical translational biomedical research
Nice to have: coordinating clinical research studies
The CRC is responsible for coordinating and assuring integrity of all activities associated with conducting TBICoE clinical investigations in the area of TBI, ensuring compliance with local, state, and federal regulatory requirements.
Compensation
The likely salary range for this position is $57,824 - $78,200.
Responsibilities
Coordinates and assures integrity of all activities associated with conducting TBICoE TBI clinical investigations
Assists Principal / Associate Investigators in the preparation and submission of clinical protocols, consent forms, and other documents
Maintains regulatory files related to TBICoE clinical investigations
Communicates with research participants, staff, regulatory affairs and data management groups, laboratory and clinical investigators
Recruits, interviews, and screens TBICoE clinical research study volunteers, administers and obtains informed consent
Requirements
Bachelor's degree or higher in biology, psychology or related science
Nice to have: Master’s degree
Nice to have: Certification as a Clinical Research Coordinator (CCRC)
Nice to have: Clinical Research Professional (CCRP)
Supports the coordination and execution of clinical and research studies under limited supervision, ensuring compliance with institutional policies, regulatory requirements, and federal regulations.
Responsibilities
Supports implementation and conduct of research studies in accordance with protocols and GCP
Maintains accurate study records and regulatory documentation
Assists with monitoring, documenting, and reporting adverse events and protocol deviations
Participates in audit preparation and regulatory reviews
Assists with recruitment, screening, enrollment, and retention of participants
Requirements
High School Diploma or G.E.D.
Associate's Degree in a healthcare, science, research, or related field
Responsible for evaluating donor eligibility, administering immunizations, providing limited emergency care, and ensuring compliance with SOPs and regulatory guidelines at a plasma center.
Responsibilities
Evaluate donor eligibility through medical history reviews, physical assessments, and informed consent discussions
Review, document, and verify donor information, immunization records, and test results in the donor management system (NexLynk)
Classify donors into appropriate programs and monitor for adverse reactions
Consult with the center Licensed Physician regarding abnormal results, donor eligibility concerns, and immunization orders
Counsel deferred donors, ensure confidentiality, and refer donors to health departments when needed
Requirements
Graduate of a recognized healthcare-related program
Nice to have: One year of experience in hospital, field care, or plasma center settings
Responsible for evaluating donor eligibility, administering immunizations, providing limited emergency care, and ensuring compliance with SOPs and regulatory guidelines at a plasma center.
Responsibilities
Evaluate donor eligibility through medical history reviews, physical assessments, and informed consent discussions
Review, document, and verify donor information, immunization records, and test results in the donor management system (NexLynk)
Classify donors into appropriate programs and monitor for adverse reactions
Consult with the center Licensed Physician regarding abnormal results, donor eligibility concerns, and immunization orders
Counsel deferred donors, ensure confidentiality, and refer donors to health departments when needed
Requirements
Graduate of a recognized healthcare-related program
Nice to have: one year of experience in hospital, field care, or plasma center settings
Responsible for evaluating donor eligibility, administering immunizations, providing limited emergency care, and ensuring compliance with SOPs and regulatory guidelines at a plasma center.
Compensation
The expected base pay for this position at hiring is $40.78-$54.38-$67.97.
Responsibilities
Evaluate donor eligibility through medical history reviews, physical assessments, and informed consent discussions
Review, document, and verify donor information, immunization records, and test results in the donor management system (NexLynk)
Classify donors into appropriate programs and monitor for adverse reactions
Consult with the center Licensed Physician regarding abnormal results, donor eligibility concerns, and immunization orders
Counsel deferred donors, ensure confidentiality, and refer donors to health departments when needed
Requirements
Graduate of a recognized healthcare-related program
Nice to have: One year of experience in hospital, field care, or plasma center settings
Manages the preparation, review and coordination of Country Submissions in line with global submission strategy.
Responsibilities
Prepares, reviews and coordinates submissions (MoH, EC, applications if, e.g. gene therapy approvals, safety dossiers, import license) in alignment with global submission strategy.
Provides strategy advice (MoH &/or EC) to clients.
Develops and implements local submission strategy.
Provides expertise and coordination oversight for projects in collaboration with relevant internal departments.
Serves as primary contact for investigators and with the local authorities to ensure submissions are managed in a timely manner.
Biological Scientist III - EndocrinologyUniversity of Florida · Gainesville, US
Medical Professional, EMTOctapharma · Durham, US