Skip to main content

Clinical Trials Specialist Oncology / Full Time / San Diego

Job ID JR132366 Date Posted 12/30/2022
San Diego, California
  • Sharp Memorial Hospital
  • Day
  • Regular
Apply now


Shift Start Time:

Shift End Time:

Additional Shift Information:

Weekend Requirements:

On-Call Required:


Hourly Pay Range (Minimum - Midpoint - Maximum):

$39.435 - $50.884 - $62.333

The stated pay scale reflects the range that Sharp reasonably expects to pay for this position.  The actual pay rate and pay grade for this position will be dependent on a variety of factors, including an applicant’s years of experience, unique skills and abilities, education, alignment with similar internal candidates, marketplace factors, other requirements for the position, and employer business practices.

What You Will Do
Conducts research, ensuring adherence to the ethical responsibilities of each assigned protocol. Assists Principal Investigators in research methodology on new continuing and proposed studies. Participates in the planning and managing of the operational budget.

Required Qualifications
  • Bachelor's Degree Health related field
  • 2 Years Research experience required (Masters degree or Ph.D/PsyD may be considered in lieu of experience)
  • Medical and/or psychiatric background

Essential Functions
  • Clinical competency and professional development

    Maintains productivity and identifies revenue enhancing opportunities.
    Represents the hospital and its research studies to the community in an ethical and professional manner.
    Maintains responsibility for recruitment of subjects.
    Attends pharmaceutical companies study coordinator conferences and obligatory orientation meetings.
    Remains available for touring visits, attending speaking engagements or any other function that promotes research studies at Sharp Mesa Vista Hospital and Sharp HealthCare.
    Belongs to, attends, and/or participates in professional related organizations.
  • Communication

    Explains to subjects the aim, method, anticipated benefits, and potential hazards and/or discomforts of study.
    Informs subjects they may withdraw consent to participate at any time and will be told which alternative treatments will be available to them.
    Provides ongoing communication with subjects to ensure compliance with protocol and prevent and/or monitor adverse events.
    Informs Principal Investigator and Research Director/Manager of all aspects of the study and conditions of the subject.
    Maintains communication between physicians participating in the study, study facilitator and subjects to identify and complete visits according to protocol schedule.
    Responds within the allotted time frame to pharmaceutical company queries regarding case record completion or other elements of the study according to protocol.
    Communicates with designated pharmaceutical company's study monitor throughout the study on any problems, issues or questions concerning the study or reporting of adverse events.
  • Documentation

    Documents each subject visits in the Case Report Form, ensuring accuracy and consistency with the clinical information in the Source Document.
    Ensures the Source Document is completed each visit and supports data entered in the Case Report Form.
    Documents and follows adverse events through to resolution to ensure patient's safety and well being.
    Ensures appropriate dispensing and accountable documentation of study medication.
  • Protocol compliance

    Conducts research studies only after full approval of the protocol obtained from the local Ethics Committee (IRB).
    Obtain Informed Consent from each subject prior to entering the study, ensuring that each patient's capacity for understanding is intact.
    Writes and presents protocol synopsis to IRB for approval.
    Prepares documents for IRB approval, i.e., protocol amendments, revised inform consents, etc.
    Performs assessments according to protocol visits, meeting inter-rater reliability standards.
    Ensures investigational drug handling is conducted according to GCP, FDA regulations and protocol.
    Accurately randomizes patients to treatment groups according to study randomization procedure.
    Assists physician in evaluating subject tolerance and dosage of study medication.

Sharp HealthCare is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability or any other protected class

Bachelor's Degree
Apply now

Want to know when new jobs are posted? Sign up for job alerts.

Set your parameters to automatically receive alerts when we post new jobs that fit your skills, interests and experience.

Sign up for job alerts

Select your area of interest from the categories below and click “Add” to receive email alerts about our latest openings. Or you can refine your job alerts by selecting a specific facility.

Interested In

Glassdoor rating Glassdoor rating

"After nearly 10 years of working here, it's still one of the hardest jobs I've ever loved. If you find a niche here, you'll be working with some of the smartest in the industry. This is where they'll respect you for thinking outside the box and kindness matters. They expect consistency and hard work, but pay you well to do it."

We are Sharp

Stay connected and join the career interest community

Want to stay informed about career opportunities and life at Sharp? Join our career interest community and receive information that matters to you.

Join the community