Onsite Clinical Research Coordinator II – Orlando

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

Paid Time Off from Day One

403-B Retirement Plan

Parental Leave (4 Weeks)

Career Development

Well-being Resources

Mental Health Resources and Support

Pet Benefits

Job summary

Actalent is seeking a Clinical Research Coordinator II in Orlando, FL for a permanent onsite role. The shift is 6:45am - 3:15pm, five days a week, with responsibilities spanning participant screening, consent, follow-up, data collection, and regulatory compliance.

The role requires a clinical research background, HIPAA knowledge, and strong organizational and communication skills. Onsite work with benefits and career development support included.

Qualifications

• Bachelor's degree with 1 year of clinical research experience or equivalent
• Associate degree with 2 years of clinical research experience
• 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

Clinical research experience

HIPAA knowledge

Organizational skills

Communication skills

Problem-solving skills

Education

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

Associate degree in related field

Accredited allied health certificate program

Tools

Microsoft Office

Job description

Actalent is seeking a Clinical Research Coordinator II in Orlando, FL for a permanent onsite role. The shift is 6:45am - 3:15pm, five days a week, with responsibilities spanning participant screening, consent, follow-up, data collection, and regulatory compliance.

The role requires a clinical research background, HIPAA knowledge, and strong organizational and communication skills. Onsite work with benefits and career development support included.