Clinical Research Coordinator

				Overview:

At St. Luke's, we pride ourselves on fostering a workplace culture that values diversity, promotes collaboration, and prioritizes employee well-being. Our commitment to excellence in patient care extends to creating an environment where our team can thrive both personally and professionally. With opportunities for growth, competitive benefits, and a supportive community of colleagues, St. Luke's is truly a great place to work.

What You Can Expect:

St. Luke's Cancer Institute Research encompasses cancer care for adult and pediatric patients, as well as blood and bleeding disorders, in outpatient and inpatient settings. The primary focus of this position is the coordination of adult clinical trials. A successful candidate will be someone who craves variety in their work and wants to integrate and collaborate with team members across multiple departments on a large variety of clinical trials.

* Conducts and documents informed consent process.
* Reviews clinical records and extracts necessary data to determine eligibility and complete data submission via the appropriate mechanism.
* Assists in recruiting patients for clinical trials.
* Conducts research activities per protocol.
* Documents research process, adverse event grading, consent process, patient progress on study in electronic medical record.
* Initiates and submits Serious Adverse Events reports to study sponsor in collaboration with the physician and/or principal investigator.
* Maintains clinical trials management system; prepare reports as needed.
* Prepares for and conducts study monitor visits and audits.
* Serves as liaison and reference to physicians, investigators, and other staff members for questions regarding the research process.
* Collaborates with investigator and regulatory staff regarding Institutional Review Board requirements.
* Prepares basic statistical reports or other reports and presentations as required.
* Collaborates with external community, business, and academic partners.
* Works constructively with coworkers and clinicians to improve processes and standards of practice.
* Perform other duties and responsibilities as assigned.

Minimum Qualifications:

* Education: Bachelor's degree
* Experience: 2 years' experience

Preferred Qualifications:

* Strong background in oncology or clinical research
* Working knowledge of medical and scientific terminology
* Experience working directly with patients

Responsibilities:

The Clinical Research Coordinator 2 is responsible for identifying eligible patients for research and ensuring that research protocols are carried out accurately.

* Conducts and documents informed consent process.
* Reviews clinical records and extracts necessary data to determine eligibility and complete data submission via the appropriate mechanism.
* Conducts research activities per protocol.
* Documents research process, adverse event grading, consent process, patient progress on study in electronic medical record.
* Initiates and submits Serious Adverse Events reports to study sponsor in collaboration with the physician and/or principal investigator.
* May maintain clinical trials management system; prepare reports as needed.
* May prepare for and conduct study monitor visits and audits.
* Serves as liaison and reference to physicians, investigators and other staff members for questions regarding the research process.
* Collaborates with investigator and regulatory staff regarding Institutional Review Board requirements.
* May participate in protocol design, development, and writing, as well as writing study manuscripts. May complete scientific literature searches and due diligence practices prior to study inception.
* Prepares basic statistical reports or other reports and presentations as required.
* Collaborates with external community, business and academic partners.
* Mentor research staff by acting as a content expert.
* Perform other duties and responsibilities as assigned.

Qualifications:

* Education: Bachelor's degree.
* Experience: 3 year's experience.
* Licenses/Certifications: None
			

Apply

Share this job:

Share this Job

View company profile

St. Luke's Health System

Connect To Our Company