Clinical Research Coordinator

START Center for Cancer Research; West Valley City (UT); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Comprehensive health coverage

401(k) with employer matching

Life and disability insurance

Flexible spending accounts

Paid time off

Job summary

The START Center for Cancer Research is seeking a Clinical Research Coordinator to support early phase oncology clinical trials under supervision of senior staff. You will ensure accurate and timely conduct, adherence to protocols, regulatory requirements, and patient safety standards.

Responsibilities include coordinating with sponsors, monitoring study activities, assisting with patient screening and consent, and maintaining source documents.

Qualifications

• High School Diploma or GED required.
• 2+ years of clinical research experience preferred.
• Strong knowledge of GCP and regulatory requirements.
• Proficiency in Microsoft Office and clinical trial management software.

Responsibilities

• Coordinate daily trial activities with sponsors, CROs, and staff to track protocol status.
• Monitor day-to-day conduct of studies per protocol, SOPs, and GCP to ensure data integrity.
• Prepare/review forms for trials to ensure protocol compliance.
• Maintain trial files with standardized labeling and filing.

Skills

Attention to detail

Communication skills

GCP knowledge

Data entry

Microsoft Office

Education

High School Diploma or GED

2 years clinical research experience

Tools

CTMS

Microsoft Office

Job description

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval.

We are hiring a Clinical Research Coordinator to work under the guidance of senior research staff to support the daily activities of early phase oncology clinical trials. The CRC ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards.

Work Schedule: Monday-Friday 8:00am-4:00pm

Location: 2965 W 3500 S #4th,West Valley City, Utah84119

Essential Responsibilities

• Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc.regardingquestions, concerns, as well as status of the protocol.
• Monitor the overall day-to-day conduct of assigned studiesin accordance withthe specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrityregardingall aspects of the study.
• Create/review forms created or revised for assigned trials toassureprotocol compliance.
• Maintainfiles using standardized study document labeling and filing procedures.
• Implement initial protocol and amendments, training staff who will be involved in patient treatment and management.
• Maintain an up-to-date contact list.
• Assistwith patient screening and determination of eligibility.
• Facilitate the informed consent process ensuring that consent is appropriately completed.
• Prepare and manage source documents according to standard operating procedures.
• Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations.
• Assistdata coordinator team with casereport formcompletion and query resolution.
• Work with the Principal Investigator to complete andsubmitSerious Adverse Event reports.
• Perform protocol specific closeout related activities in conjunction with the data coordinator.
• Provide documentation for alldeviationswhether related to the protocol or a SOP.
• Ensure that all team members involved understand and adhere to assigned protocols.
• Perform telephone triage assessments of patients on trial when necessary.
• Provide patient education regarding participation in a clinical trial, chemotherapy/biotherapy/investigational agent administration and potential side effects.

Required Education and Experience:

• High School Diploma or GED.
• 2 years of clinical research experience.
• Basic understanding of oncology clinical trials, particularly Phase 1 studies.
• Strong attention to detail and accuracy in data collection and documentation.
• Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
• Working knowledge of GCP and regulatory requirements.
• Proficient in Microsoft Office Suite and clinical trial management software.

Preferred Education and Experience:

• Experience working in an oncology setting.

Physical & Travel Requirements:

• Approximately 80% oftimeis spent sitting.
• Very fast-paced and ever-changing healthcare environment.
• Demanding deadlines andtime frames.
• Constant demand for updating knowledge.
• Works closely with physicians and ancillary personnel in caring for and treating oncology/hematology patients.

Best-in-Class Benefits and Perks

We value our employees’ time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

• Comprehensive health coverage: Medical, dental, and vision insurance provided
• Robust retirement planning: 401(k) plan available with employer matching
• Financial security: Life and disability insurance for added protection
• Flexible financial options: Health savings and flexible spending accounts offered
• Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
• Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research

Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world.

Learn more atSTARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?

Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.