Clinical Research Coordinator II

Actalent; Orlando (FL); On-site; USD 64,000 - 73,000; Full time

Benefits offered by this job

Medical, Dental, Vision Insurance

Life Insurance

Disability Insurance

PTO from Day One

403-B Retirement Plan

4 Weeks Paid Parental Leave

Career Development

Whole Person Well-being Resources

Mental Health Resources and Support

Pet Benefits

Job summary

Actalent is seeking a Clinical Research Coordinator for a permanent, onsite role in Orlando, FL. The candidate will screen, recruit, consent, and coordinate participants for clinical studies, while managing follow-up and biospecimen collection across the research lifecycle.

The role requires a healthcare/clinical research background, knowledge of HIPAA and ethics, attention to detail, and the ability to handle multiple priorities in a fast-paced setting. Onsite benefits are provided.

Qualifications

• Bachelor's degree in Healthcare Administration, Clinical Research, Life Sciences, or related field with 1 year of clinical research experience
• OR Associate degree in a related field with 2 years of clinical research experience
• OR Accredited allied health certificate program with 4 years of clinical research experience
• Clinical research experience
• Knowledge of HIPAA, patient privacy, and research ethics
• Strong organizational, communication, and problem-solving skills
• Ability to manage multiple priorities in a fast-paced environment
• Proficiency with Microsoft Office (Word, Excel, Outlook)

Responsibilities

• Screen, recruit, consent, and coordinate research participants for clinical studies
• Manage participant follow-up and study-related activities throughout the research lifecycle
• Coordinate or perform biospecimen collection and research data collection
• Maintain accurate research records and HIPAA-compliant databases
• Serve as the primary point of contact for participants, investigators, and study teams
• Collaborate with clinical, laboratory, and hospital departments to ensure protocol and regulatory compliance
• Support data entry, reporting, and research documentation activities
• Assist with protocol implementation and adherence to SOPs and research standards

Skills

HIPAA knowledge

Organizational skills

Communication skills

Problem-solving skills

Ability to manage multiple priorities

Education

Bachelor's degree in Healthcare Administration, Clinical Research, Life Sciences, or related field

Associate degree in a related field

Allied health certificate program

Tools

Microsoft Office (Word, Excel, Outlook)

Job description

Hours: 6:45am - 3:15pm, 5 days a week onsite

Location: Multiple Locations (Travel Between Sites Required)

Required Qualifications

• Bachelor's degree in Healthcare Administration, Clinical Research, Life Sciences, or related field with 1 year of clinical research experience ;
• OR
• Associate degree in a related field with 2 years of clinical research experience;
• OR
• Accredited allied health certificate program with 4 years of clinical research experience
• Clinical research experience
• Knowledge of HIPAA, patient privacy, and research ethics
• Strong organizational, communication, and problem-solving skills
• Ability to manage multiple priorities in a fast-paced environment
• Proficiency with Microsoft Office (Word, Excel, Outlook)

Key Responsibilities

• Screen, recruit, consent, and coordinate research participants for clinical studies
• Manage participant follow-up and study-related activities throughout the research lifecycle
• Coordinate or perform biospecimen collection and research data collection
• Maintain accurate research records and HIPAA-compliant databases
• Serve as the primary point of contact for participants, investigators, and study teams
• Collaborate with clinical, laboratory, and hospital departments to ensure protocol and regulatory compliance
• Support data entry, reporting, and research documentation activities
• Assist with protocol implementation and adherence to SOPs and research standards

Job Type & Location

This is a Permanent position based out of Orlando, FL.

Pay And Benefits

The pay range for this position is $64480.00 - $72800.00/yr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

• Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance Paid Time Off from Day One 403-B Retirement Plan 4 Weeks 100% Paid Parental Leave Career Development Whole Person Well-being Resources Mental Health Resources and Support Pet Benefits

Job Type & Location

This is a Permanent position based out of Orlando, FL.

Application Deadline

This position is anticipated to close on Nov 5, 2026.

Workplace Type

This is a fully onsite position in Orlando,FL.

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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: 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.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.