On-Site Clinical Trials Recruiter

Bio Behavioral Health Inc; Toms River (NJ); Presencial; USD 60.000 - 85.000; Tempo integral

Benefícios oferecidos por esta vaga

Medical, dental, and vision coverage

Health Savings Account (HSA) and FSA

Company-paid life and disability保险

401(k) retirement plan with company-mt

Paid time off and holidays

Employee Assistance Program (EAP)

Resumo da vaga

PhaseWell Research is seeking a detail-oriented Recruitment Specialist to support start-up and enrollment phases of clinical trials. You will conduct direct participant outreach, qualify potential participants, and maintain recruitment data in CTMS/CRIO and Excel.

You will collaborate with clinical staff, sponsors, and study participants, reporting to the Recruitment Manager. The role requires strong communication, CRM proficiency, and the ability to work onsite in New Jersey with local travel

Qualificações

• Bachelor's degree preferred (health/marketing) or equivalent experience.
• Experience in clinical research recruitment or sales is preferred.
• Knowledge of CRM systems and prospect tracking is required.
• Strong communication and outreach skills are essential.

Responsabilidades

• Direct participant outreach via phone, text, email, or in person to explain study opportunities.
• Maintain recruitment data and CTMS/CRIO entries accurately.
• Collaborate with clinical and administrative staff, sponsors, and participants.
• Attend start-up and recruitment plan meetings and contribute to strategy.

Conhecimentos

CRM knowledge

Telemarketing/sales experience

Communication & interpersonal

MS Office proficiency

Formação

Bachelor's degree preferred (health/marketing)

Ferramentas

CRIO/CTMS familiarity

CRM platforms

Descrição da vaga

PhaseWell Research is seeking a detail-oriented Recruitment Specialist to support start-up and enrollment phases of clinical trials. You will conduct direct participant outreach, qualify potential participants, and maintain recruitment data in CTMS/CRIO and Excel.

You will collaborate with clinical staff, sponsors, and study participants, reporting to the Recruitment Manager. The role requires strong communication, CRM proficiency, and the ability to work onsite in New Jersey with local travel