Clinical Research Coordinator (CRC)

Location: Lufkin, TX
Pay: Up to $32/hour
Type: Contract
Contract Duration: Through March 31, 2027, with potential for extension based on study and business needs
Schedule: Onsite

About the Opportunity

Adecco Healthcare & Life Sciences is partnering with an established clinical research organization to hire an experienced Clinical Research Coordinator (CRC) to support an ongoing clinical study in Lufkin, Texas.

This is an excellent opportunity for a CRC who enjoys a combination of patient coordination, clinical research operations, data entry, documentation, and study support. The ideal candidate will bring previous clinical research experience, strong attention to detail, and the ability to collaborate effectively with investigators, patients, sponsors, and other stakeholders.

What You’ll Do

• Conduct clinical study activities in accordance with FDA regulations, Good Clinical Practice (GCP), ICH guidelines, study protocols, and applicable SOPs.

• Accurately record patient information, test results, and study-related data in required documentation and systems.

• Perform clinical research data entry and maintain accurate electronic case report forms (eCRFs) and electronic data capture (EDC) records.

• Review study information for accuracy and completeness and assist with query resolution within required timelines.

• Gather, maintain, and update source documents, patient files, and study notes.

• Support patient scheduling, appointment coordination, follow-up calls, and other patient-facing activities as needed.

• Build positive relationships with study participants and support patient engagement and retention.

• Attend site initiation meetings, protocol training, investigator meetings, and other relevant study meetings.

• Complete investigational product (IP) accountability documentation when applicable.

• Identify and appropriately report potential protocol or regulatory non-compliance.

• Support IRB requirements and ensure applicable approvals and ongoing requirements are maintained.

• Ensure study information is accurately entered into sponsor systems and completed within established timelines.

• Handle sensitive patient and study information with appropriate discretion and confidentiality.

• Follow applicable company policies, procedures, and clinical research standards.

• Contribute to a professional, organized, and compliant research environment.

What We’re Looking For

• Bachelor’s degree or equivalent education and relevant clinical/medical training.

• 2+ years of relevant clinical research experience, ideally in a Clinical Research Coordinator or comparable role.

• Previous experience supporting clinical trials and working directly with study protocols.

• Solid understanding of GCP, SOPs, informed consent, safety monitoring, and clinical research regulations.

• Experience with EDC systems, clinical research data entry, eCRFs, and query resolution.

• Strong organizational skills and exceptional attention to detail.

• Ability to work independently while collaborating effectively with a multidisciplinary team.

• Strong problem-solving, decision-making, and prioritization skills.

• Professional communication and interpersonal skills.

• Ability to exercise sound judgment and discretion when handling confidential information.

• Proficiency with standard computer applications and clinical research systems.

• Ability to adapt to changing priorities and work effectively with different stakeholders.

Why Consider This Opportunity?

• Up to $32/hour, based on qualifications and experience.

• Contract opportunity through March 31, 2027.

• Potential for extension based on study needs and business requirements.

• Opportunity to contribute to an active clinical research study.

• Hands-on exposure across clinical trial coordination, patient interaction, data management, and study documentation.

• Collaborative environment with opportunities to work closely with clinical research and study stakeholders.

Work Location

Lufkin, Texas – 100% Onsite

This position requires onsite work at the clinical research site.

About Adecco Healthcare & Life Sciences

Adecco Healthcare & Life Sciences connects qualified professionals with opportunities across clinical research, healthcare, pharmaceutical, biotechnology, and life sciences organizations.

Eligible associates may have access to weekly pay, benefits, 401(k), paid time off and holiday eligibility, skills training, and other resources based on assignment and eligibility.

Adecco is an Equal Opportunity Employer.

Pay Details: $28.00 to $32.00 per hour

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

Military connected talent encouraged to apply

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The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

• The California Fair Chance Act
• Los Angeles City Fair Chance Ordinance
• Los Angeles County Fair Chance Ordinance for Employers
• San Francisco Fair Chance Ordinance

Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.