Top 19 Clinical research associate Jobs in Fort Worth Tx

Clinical Research Coordinator
START Center for Cancer Research —Fort Worth, TX
- Monday to Friday
- Mid-level
- High school diploma or GED
- 2 years
- Health savings account
- Paid holidays
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Clinical Research Coordinator
PRIME CLINICAL RESEARCH INC —Mansfield, TX
- Full-time
- Mid-level
- Bachelor's degree
- Organizational skills
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CRA 1, IQVIA Biotech
IQVIA —Fort Worth, TX
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
Research Coordinator
IQVIA —Irving, TX
- $43,400 - $108,200 a year
- Full-time
- Nursing
- RN License
- 5 years
Clinical Research RN - Full time
Texas Health Resources —Fort Worth, TX
- Weekends as needed
- Nursing
- RN License
- Hospital
- Paid parental leave
- Health insurance
Data Coordinator
START Center for Cancer Research —Fort Worth, TX
- Monday to Friday
- Mid-level
- High school diploma or GED
- Bachelor's degree
- Health savings account
- Paid holidays
Quick Apply
9d
CTMS Entry Coordinator
START Center for Cancer Research —Fort Worth, TX
- Monday to Friday
- Office
- Administrative experience
- High school diploma or GED
- Health savings account
- Paid holidays
Quick Apply
10d
Research Site Manager
Iterative Health —Southlake, TX
- Inventory management
- Mid-level
- Clinic
Clinical Research Coordinator II - Nurse
Iterative Health —Mansfield, TX
- Full-time
- Nursing
- RN License
- Mid-level
Quick Apply
Clinical Research Unit Manager
Texas A&M AgriLife —Fort Worth, TX
- Full-time
- Spanish
- CPR Certification
- Nursing
Senior Manager, Clinical Operations - Cardiology
Iterative Health —Southlake, TX
- $140,000 - $165,000 a year
- Hybrid work
- 5 years
- Office
- Analysis skills
- Health savings account
- Disability insurance
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Principal Investigator - (MD/DO)
DM CLINICAL RESEARCH GROUP —Irving, TX
- $90 - $130 an hour
- Medicine
- BC/BE
- Writing skills

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CRA 1, IQVIA Biotech
IQVIA —Fort Worth, TX
During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the…
$71,900 - $145,300 a year
CRA 2/Senior CRA
IQVIA —Dallas, TX
Bachelor’s degree in life sciences, healthcare, or related field (or equivalent experience). In this role, you’ll partner with investigative sites and cross-…
$90,200 - $175,100 a year

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Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…
Clinical Research Coordinator I
Nationwide Children's Hospital —Columbus, OH
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…

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Clinical Research Coordinator

START Center for Cancer Research -
Fort Worth, TX

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Job Details

Benefits

Health savings account
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Employee assistance program
Vision insurance
401(k) matching

Qualifications

Medical software
Regulatory compliance
High school diploma or GED
Oncology research
Patient interaction
Productivity software
Clinical quality assurance standards

Full Job Description

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access” to cutting edge trials throughout the United States and 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. Also, this role is responsible for implementation as well as completion of protocol specific requirements, providing accurate, up to date information to all team members involved with any aspect of carrying out protocol specific requirements.

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

Location: 900 W. Magnolia Ave., Fort Worth, Texas 76104

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.
Maintain an up-to-date contact list.
Assist with 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.
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.
Perform protocol specific closeout related activities in conjunction with the data coordinator.
Provide documentation for all deviations whether related to the protocol or a SOP.
Ensure that all team members involved understand and adhere to assigned protocols.

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.
Excellent organizational and time-management skills.
Strong communication skills, both written and verbal.
Ability to interact professionally with patients, study staff, and external stakeholders.
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

We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally:

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 coverage and optional insurance options

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’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join 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. START represents the 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.

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. Please submit your application online.

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.

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clinical research associate jobs in fort worth tx

Clinical Research Coordinator

Clinical Research Coordinator

CRA 1, IQVIA Biotech

Research Coordinator

Clinical Research RN - Full time

Data Coordinator

CTMS Entry Coordinator

Research Site Manager

Clinical Research Coordinator II - Nurse

Clinical Research Unit Manager

Senior Manager, Clinical Operations - Cardiology

Principal Investigator - (MD/DO)

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