Conduct onsite monitoring across clinical studies, oversee site communication and study progress, review clinical data, resolve queries, and support study startup and regulatory submissions.
Clinical Trial Liaison (Oncology)
📜 Description
- Provide protocol-tailored support to sites to improve patient identification and recruitment.
- Help sites develop and implement patient enrollment techniques.
- Coordinate site-specific recruitment and retention plans against planned metrics.
- Share oncology expertise with site team members involved in patient recruitment.
- Track and report patient enrollment progress throughout the study.
- Analyze protocols and support patient pathways, study documentation, and site monitors.
🛠️ Requirements
- Registered Nurse (RN) Degree
- A minimum of 5 years of experience in Oncology
- Experience in operation and QC procedures related to the equipment used on Oncology research studies
- Previous experience in at least one of following areas is preferred:CAR-T cell therapyHematology (Leukemia/Lymphoma, Myeloma, etc.)Solid TumorRadiopharmaceuticals
- Previous experience in clinical research is preferred
Full job description
Company Description
PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
We are looking for a nurse with experience in clinical research and Oncology studies to join our team!
In this role, a Clinical Trial Liaison:
- Acts as a specialized liaison to assist sites with a protocol-tailored approach to increase efficiency of the patient identification and recruitment process
- Assists sites in developing and implementing patient enrollment techniques
- Coordinates site specific patient recruitment and retention plans observing the planned metrics
- Provides information specific to the area of expertise to site team members involved in patient recruitment
- Identifies, tracks, and reports patient enrollment progress throughout the study
- Analyses the protocol in order to provide the site with the support needed to improve the patient pathway
- Provides support to the project teams to ensure proper documentation of study-specific assessments related to patient enrollment
- Assists and advises the site monitor in the area of patient enrollment
This role requires approximately 35% travel.
Qualifications
- Registered Nurse (RN) Degree
- A minimum of 5 years of experience in Oncology
- Experience in operation and QC procedures related to the equipment used on Oncology research studies
- Previous experience in at least one of following areas is preferred:
- CAR-T cell therapy
- Hematology (Leukemia/Lymphoma, Myeloma, etc.)
- Solid Tumor
- Radiopharmaceuticals
- Previous experience in clinical research is preferred
For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future.
Additional Information
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
Similar jobs
Search more Clinical Research Specialist jobsConduct clinical trial site monitoring from selection through closeout, support investigators and study teams with training and communication, and help maintain study quality, documentation, and progress.
Conduct onsite monitoring across Phase II and III clinical studies, manage site communications and study documentation, and coordinate with project teams, vendors, and support services.
Build and manage a country-specific network of referring physicians, supporting effective referrals to study investigators through physician training, regular engagement, and cross-functional collaboration.
Apply clinical and scientific expertise to human health consulting matters, researching and evaluating evidence and helping prepare reports for legal, insurance, and other clients.
