Clinical Research Coordinator at Actalent Harlingen, TX
26 an hour
Behavioral Health Market Context
Apply Nowvia Majorette Events
Benefits
Health InsuranceDental CoveragePaid Time Off
Job Description
rate with clinical teams and principal investigators to conduct clinical trials effectively.
• Serve as a liaison between patients, families, clinical staff, and pharmaceutical sponsors.
• Monitor patients during research procedures and ensure accurate documentation.
• Maintain integrity and accuracy of clinical trial data and records.
• Report serious adverse events and study updates to appropriate parties.
• Coordinate interdepartmental research efforts and promote staff awareness of clinical trial requirements.
• Participate in study development, including protocol review, consent form preparation, and regulatory submissions.
• Lead and support multiple clinical trials through project management and relationship development.
Required Skills & Experience:
• Clinical trial coordination experience required.
• Patient recruitment experience required.
Qualifications:
• Minimum Education: Bachelor’s degree in a health-related field
Pay and Benefits
The pay range for this position is $26.93 - $38.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Harlingen,TX.
Application Deadline
This position is anticipated to close on Nov 7, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] for other accommodation options.
• Serve as a liaison between patients, families, clinical staff, and pharmaceutical sponsors.
• Monitor patients during research procedures and ensure accurate documentation.
• Maintain integrity and accuracy of clinical trial data and records.
• Report serious adverse events and study updates to appropriate parties.
• Coordinate interdepartmental research efforts and promote staff awareness of clinical trial requirements.
• Participate in study development, including protocol review, consent form preparation, and regulatory submissions.
• Lead and support multiple clinical trials through project management and relationship development.
Required Skills & Experience:
• Clinical trial coordination experience required.
• Patient recruitment experience required.
Qualifications:
• Minimum Education: Bachelor’s degree in a health-related field
Pay and Benefits
The pay range for this position is $26.93 - $38.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Harlingen,TX.
Application Deadline
This position is anticipated to close on Nov 7, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] for other accommodation options.
Qualifications
- •Clinical trial coordination experience required
- •Patient recruitment experience required
- •Minimum Education: Bachelor’s degree in a health-related field
Benefits
- •Pay and Benefits
- •The pay range for this position is $26.93 - $38.00/hr
- •subject to specific elections, plan, or program terms
- •Medical, dental & vision
- •Critical Illness, Accident, and Hospital
- •401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
- •Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- •Short and long-term disability
- •Health Spending Account (HSA)
- •Transportation benefits
- •Employee Assistance Program
- •Time Off/Leave (PTO, Vacation or Sick Leave)
Responsibilities
- •Collect and enter data for research projects and protocols in compliance with regulatory and institutional standards
- •Collaborate with clinical teams and principal investigators to conduct clinical trials effectively
- •Serve as a liaison between patients, families, clinical staff, and pharmaceutical sponsors
- •Monitor patients during research procedures and ensure accurate documentation
- •Maintain integrity and accuracy of clinical trial data and records
- •Report serious adverse events and study updates to appropriate parties
- •Coordinate interdepartmental research efforts and promote staff awareness of clinical trial requirements
- •Participate in study development, including protocol review, consent form preparation, and regulatory submissions
- •Lead and support multiple clinical trials through project management and relationship development
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