Clinical Research Coordinator
West Lafayette, INFull-time
Behavioral Health Market Context
Apply Nowvia Talents By Vaia
Benefits
Paid Time OffDental CoverageHealth Insurance
Job Description
lopment and implementation of clinical study protocols, coordinating participant recruitment, and managing daily operations of clinical trials. The ideal candidate will have strong experience in clinical research or healthcare, with a preference for those with phlebotomy experience.
Responsibilities
• Assist in the development and implementation of clinical study protocols.
• Coordinate participant recruitment, screening, and enrollment.
• Manage daily operations of clinical trials, including scheduling and conducting participant visits.
• Serve as a liaison between study participants, investigators, and other healthcare professionals.
• Monitor study progress and report any issues or adverse events to the Principal Investigator and relevant authorities.
Essential Skills
• Phlebotomy experience is highly preferred.
• Previous experience in clinical research or healthcare.
• Strong organizational and communication skills.
• Ability to work independently and as part of a team.
Additional Skills & Qualifications
• Bachelor's degree in a related field preferred (e.g., life sciences, nursing, public health), but a minimum of a high school diploma is required.
• Experience in patient recruitment, pre-screening, and clinical research, especially in dermatology.
Work Environment
This is a fully onsite position, operating Monday through Friday from 8 am to 5 pm EST.
Job Type & Location
This is a Contract to Hire position based out of West Lafayette, Indiana.
Pay and Benefits
The pay range for this position is $21.00 - $28.00/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 West Lafayette,IN.
Application Deadline
This position is anticipated to close on Oct 17, 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.
Responsibilities
• Assist in the development and implementation of clinical study protocols.
• Coordinate participant recruitment, screening, and enrollment.
• Manage daily operations of clinical trials, including scheduling and conducting participant visits.
• Serve as a liaison between study participants, investigators, and other healthcare professionals.
• Monitor study progress and report any issues or adverse events to the Principal Investigator and relevant authorities.
Essential Skills
• Phlebotomy experience is highly preferred.
• Previous experience in clinical research or healthcare.
• Strong organizational and communication skills.
• Ability to work independently and as part of a team.
Additional Skills & Qualifications
• Bachelor's degree in a related field preferred (e.g., life sciences, nursing, public health), but a minimum of a high school diploma is required.
• Experience in patient recruitment, pre-screening, and clinical research, especially in dermatology.
Work Environment
This is a fully onsite position, operating Monday through Friday from 8 am to 5 pm EST.
Job Type & Location
This is a Contract to Hire position based out of West Lafayette, Indiana.
Pay and Benefits
The pay range for this position is $21.00 - $28.00/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 West Lafayette,IN.
Application Deadline
This position is anticipated to close on Oct 17, 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
- •*Great opportunity to get into clinical research with NO PRIOR experience needed!
- •The ideal candidate will have strong experience in clinical research or healthcare, with a preference for those with phlebotomy experience
- •Previous experience in clinical research or healthcare
- •Strong organizational and communication skills
- •Ability to work independently and as part of a team
- •Experience in patient recruitment, pre-screening, and clinical research, especially in dermatology
Benefits
- •Pay and Benefits
- •The pay range for this position is $21.00 - $28.00/hr
- •Eligibility requirements apply to some benefits and may depend on your job
- •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
- •We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team
- •This role involves assisting in the development and implementation of clinical study protocols, coordinating participant recruitment, and managing daily operations of clinical trials
- •Assist in the development and implementation of clinical study protocols
- •Coordinate participant recruitment, screening, and enrollment
- •Manage daily operations of clinical trials, including scheduling and conducting participant visits
- •Serve as a liaison between study participants, investigators, and other healthcare professionals
- •Monitor study progress and report any issues or adverse events to the Principal Investigator and relevant authorities
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