Onsite Clinical Research Coordinator II — Coordination

Actalent; Orlando (FL); Presencial; USD 64.000 - 73.000; Tempo integral

Benefícios oferecidos por esta vaga

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

Resumo da vaga

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.

Qualificações

• 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)

Responsabilidades

• 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

Conhecimentos

HIPAA knowledge

Organizational skills

Communication skills

Problem-solving skills

Ability to manage multiple priorities

Formação

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

Associate degree in a related field

Allied health certificate program

Ferramentas

Microsoft Office (Word, Excel, Outlook)

Descrição da vaga

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.