Job Title: Clinical Research Associate
Location: New York, NY, USA

About Us:
Leoforce is the innovative company behind the AI-powered Recruiting Agent that revolutionizes talent discovery and engagement. We are passionate about empowering recruiters and job seekers with responsible AI that delivers unbiased, data-driven results. Our workplace is built on respect, integrity, and the freedom to innovate.

Why Join Leoforce?

• Career Growth: Opportunities for professional and personal advancement in a rapidly evolving industry.
• Cutting-Edge Technology: Be part of a team working on revolutionary AI solutions that redefine talent acquisition.
• Collaborative Environment: A culture that values diversity, creativity, and high performance.
• Employee Empowerment: Freedom to innovate and make a difference while being supported by a team that values respect and integrity.

Position Summary:
We are seeking a detail-oriented and motivated Clinical Research Associate to join our team. The ideal candidate will have a strong background in the healthcare domain, hands-on experience in clinical research or clinical trials, and a solid understanding of research and regulatory requirements.

Key Responsibilities:

• Oversee and monitor clinical trials to ensure compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Collaborate with investigators, site staff, and cross-functional teams to ensure the successful execution of clinical studies.
• Conduct site visits, including initiation, monitoring, and close-out visits.
• Review and verify clinical trial data and documentation for accuracy and completeness.
• Assist in the preparation and submission of regulatory documents and reports.
• Identify and resolve issues that may impact study timelines or quality.
• Maintain up-to-date knowledge of relevant research and regulatory developments.

Qualifications:

• Bachelor’s degree in life sciences, healthcare, or a related field.
• 2–5 years of experience in clinical research, clinical trials, or a related healthcare domain.
• Strong knowledge of research methodologies, regulatory requirements, and GCP guidelines.
• Excellent organizational, communication, and problem-solving skills.
• Ability to work independently and collaboratively in a fast-paced environment.
• Attention to detail and a commitment to high-quality work.

Preferred Experience:

• Experience with various therapeutic areas is a plus.
• Familiarity with electronic data capture (EDC) systems and clinical trial management systems (CTMS).

Benefits:

• Competitive compensation and benefits package.
• Opportunities for career advancement and professional development.
• Supportive and innovative work environment.

Leoforce is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.