Onderzoeker en studiecoördinator voor de PUMP-IT studie, gericht op behandeling van stadium IV colorectaal carcinoom.
Compensation
Een bruto maandsalaris tussen € 4,346,- en € 4,914,-, op basis van een 36-urige werkweek, passend bij Klinische OIO schaal en afhankelijk van je ervaring;
Responsibilities
Coördineren van de dagelijkse uitvoering van de PUMP-IT studie in meerdere Nederlandse centra
Fungeren als aanspreekpunt voor patiënten, behandelteams en externe partijen
Bewaken van inclusie, planning, protocolnaleving, datakwaliteit en rapportages
Opzetten en uitvoeren van (deel)analyses binnen het promotietraject
Schrijven van abstracts en manuscripten als basis voor een proefschrift
Advocate for patient safety and protocol integrity in clinical trials, ensuring compliance, data integrity, and effective communication among study teams.
Compensation
The potential base pay range for this role, when annualized, is $43,400.00 - $108,200.00.
Responsibilities
Advocate for patient safety and protocol integrity
Ensure protocol compliance and adherence to regulations
Collaborate with investigators, pharmacy, and clinical staff
Provide protocol-specific education to clinical staff
Facilitate and participate in study meetings and teleconferences
Requirements
Bachelor's degree required for non-RNs
Current Texas or Virginia Registered Nursing License for RNs
The Clinical Program Manager provides clinical support and administrative direction for early phase clinical trials within the Tisch Cancer Center and the Department of Immunology and Immunotherapy.
Compensation
The salary range for the role is $115494 - $192328 Annually.
Responsibilities
Supervises Clinical Research Coordinator positions and other CRNs to ensure protocol compliance, accurate data collection and sample acquisition
Develops educational programs for the Nursing Staff regarding specific protocols
Manage clinical trials portfolio and assure timely regulatory start-up of protocols
Monitor accruals and identify opportunities to grow research program
Collect and process blood specimens, administer oral solutions, and maintain phlebotomy logs while ensuring compliance with protocols and accurate data entry.
Compensation
Pay range: $23.15 - $25.85 / hour
Responsibilities
Collect specimens according to established procedures
Administer oral solutions
Research test/client information and confirm orders using lab technology systems
Navigate a computer and accurately enter data
Obtain identification and enter billing information
Requirements
High school diploma or equivalent
Nice to have: Medical assistant or paramedic training
Coordinate clinical trials at Moffitt Cancer Center, enrolling and managing patients, ensuring protocol compliance, and liaising with investigators and sponsors.
Compensation
$29.05 - $44.28
Responsibilities
Coordinate patient care and protocol compliance
Screen, enroll, and follow study subjects
Act as liaison between investigators, care providers, regulatory staff, and sponsors
Document procedures in accordance with standards and regulatory guidelines
The Oncology Research Nursing Professional (ORNP) is a Registered Nurse (RN) who works with clinical research staff to coordinate care for patients enrolled in cancer center clinical research trials, acting as a research expert for multi-disciplinary teams.
Compensation
Base Pay Scale: Generally starting at $86.50 - $114.61 per hour
Responsibilities
Collaborates with investigators on study patient screening, eligibility determination, and enrollment assessments
Uses independent judgement to assess, identify, and prioritize clinical information for clinicians
Assesses and documents signs and symptoms of illness, reactions to treatment, and changes in condition in accordance with research protocol
Manage and communicate patient/family phone calls in collaboration with medical staff
Collaborates with CRC to ensure therapeutic clinical trial flags are placed during active treatment
Requirements
BSN higher-level nursing degree
MSN (highly preferred)
Masters in research or healthcare related field (preferred)
Nice to have: 3+ years in an oncology research nurse role
The Clinical Research Assistant supports clinical research activities under the direction of senior team members, including participant recruitment, data collection, and protocol compliance.
Compensation
Pay Range $20.83 - $34.71
Responsibilities
Identifying eligible participants under supervision
Preparing necessary documents, equipment, and supplies for research visits
Conducting and documenting visits and protocol-specific testing/interviews
Maintaining study documents and regulatory binders
Managing study materials and participant logs
Requirements
BA/BS degree in a science, technical, health-related field or another applicable discipline
Clinical Research AssociateNewHologic Careers · Sweden+1 more
Mammography TechnologistRadNet, Inc. · Murrieta, US
Clinical Program Manager, Early Phase Clinical Trials Unit (RN or NP Required) - Tisch Cancer CenterMount Sinai Health System · New York, US
Phlebotomist IQuest Diagnostics · Vacaville, US
Clinical Research AssistantChildren's National Hospital (Children's National Medical Center) · Washington, US