Clinical Research Coordinator

The START Center for Cancer Research; Fort Worth (TX); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401(k) match

Annual performance bonus

PTO and paid holidays

Medical, dental, and vision coverage

Life and disability insurance

Employee Assistance Program (EAP)

Flexible Spending Accounts (FSA/HSA)

Job summary

The START Center for Cancer Research in Fort Worth, Texas is seeking a Clinical Research Coordinator to support daily activities of early-phase oncology trials. You will ensure protocol adherence, data integrity, and patient safety under supervision.

This role involves direct patient interaction and coordination across multiple protocols. Responsibilities include monitoring studies per GCP, training staff, assisting with screenings and consent, and collaborating with the PI on SAE reporting.

Qualifications

• 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.
• Working knowledge of GCP and regulatory requirements.
• Proficient in Microsoft Office Suite and clinical trial management software.

Responsibilities

• Communicate regularly with sponsors, CROs, and staff regarding protocol status and questions.
• Monitor day-to-day conduct of studies per protocol requirements and GCP.
• Create/review forms for trials to assure protocol compliance.
• Maintain study files with standardized labeling and filing procedures.
• Train staff on protocol implementation and patient management.
• Assist with patient screening and eligibility determination.
• Facilitate informed consent process ensuring proper completion.
• Identify deviations and coordinate corrective actions with leadership.
• Assist data team with case report forms and query resolution.
• Collaborate with Principal Investigator to submit Serious Adverse Event reports.

Skills

GCP knowledge

MS Office

Data collection

Oncology trials knowledge

Education

High School Diploma or GED

2 years clinical research experience

Tools

Clinical trial management software

Job description

The START Center for Cancer Research (“START”) is the world’s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering\"Hope Through Access”tocutting edgetrials throughout the UnitedStatesand Europe.

We are currently hiring a Clinical Research Coordinator. The Clinical Research Coordinator (CRC) will 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. This role involves direct patient interaction, data collection, and maintaining compliance with Good Clinical Practice (GCP). The Clinical Research Coordinator will be assigned multiple protocols at any time for which they will oversee the aspects of assigned protocols with planning and coordinating patient participation in the trial.

Work Schedule: Monday-Friday 8:00am-5:00pm

Location: 900 W. Magnolia Ave., Fort Worth, Texas76104

Essential Responsibilities:

• Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc. regarding questions, concerns, as well as status of the protocol.
• Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study.
• Create/review forms created or revised for assigned trials to assure protocol compliance.
• Maintain files using standardized study document labeling and filing procedures.
• Implement initial protocol and amendments, training staff who will be involved in patient treatment and management.
• Assist with patient screening and determination of eligibility.
• Facilitate the informed consent process ensuring that consent is appropriately completed.
• Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations.
• Assist data coordinator team with case report form completion and query resolution.
• Work with the Principal Investigator to complete and submit Serious Adverse Event reports.

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.
• 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.

Best-in-Class Benefits and Perks

• 401(k) retirement savings plan with employer match

• Eligibility for an annual performance bonus, based on role and company results

• Generous paid time off and paid holidays

• Comprehensive medical, dental, and vision coverageand optional insuranceoptions

• Company paid life and disability insurance for added financial protection

• Employee Assistance Program (EAP) providing confidential, no‑cost support for you and your family from day one

• Flexible FSA and HSA plans to support your financial wellness

• Commitment to a supportive environment that values balance, wellbeing, and flexibility

• We’recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you’lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

More About START

START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”.

Learn more at STARTresearch.com.

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.