Clinical Trials Technician

JOB TITLE:

Clinical Trial Technician

Coordinate and participate in clinical research studies conducted by principal investigators at Nebraska Hematology-Oncology, PC, performing clinical trial patient specific procedures including phlebotomy, specimen processing, electrocardiograms, and vital signs across multiple studies in accordance to appropriate regulations, Standard Operating Procedures, and study specific protocols/manuals.

Requires full range of motion including manual and finger dexterity and eye-hand coordination. Frequent standing and walking required for extended periods of time. Lifts and carries items weighing up to 50 pounds. Requires visual acuity and normal color perception.

Clinical Trials Manager

At least 1 year of experience as a phlebotomist. Clinical research experience in the collection and processing of lab samples, EKGs, vital signs preferred.

• Perform clinical trial procedures for clinical research studies conducted by principal investigator(s) at Nebraska Hematology-Oncology, PC.
• Participate in study initiation visits, source document creation/review, planning for cross-departmental procedures (such as with laboratory and sample collection from vascular access devices)
• Confirm study visit lab orders are accurate in preparation for visit
• Ensure billing compliance for study-related lab testing
• Perform study lab collection including phlebotomy, lab sample processing, storage, packaging and shipment across multiple studies simultaneously
• Perform vital signs collection and electrocardiograms in collaboration with clinical trials coordinators
• Assess/facilitate study-specific patient reported outcomes/diary compliance in collaboration with clinical trials coordinators
• Assure compliance of general and study specific processes with SOPs, the FDA, and applicable regulatory agencies.
• Perform other related duties incidental to the work described herein.
• Perform phlebotomy if/as needed for routine patient care

• Applicant should be detail-oriented with excellent communication skills.
• Position will require interaction with patients, study sponsors, the research team, and principal investigators.
• Knowledge of organizational policies, regulations, and procedures to administer clinical research protocols.
• Knowledge of medical terminology.
• Knowledge of common safety hazards and precautions to establish a safe work environment.
• Skill in identifying problems and recommending solutions.
• Skill in preparing and maintaining records, writing reports, and responding to correspondence.
• Skill in developing and maintaining department quality assurance.
• Skill in establishing and maintaining effective working relationships with patients, medical staff, and the public.
• Ability to maintain quality control standards.
• Ability to react calmly and effectively in emergency situations.
• Ability to interpret, adapt, and apply guidelines and procedures.
• Ability to communicate clearly.
• Knowledge of safety requirements and ability to recognize and correct hazardous conditions.