Clinical Trial Site Lead: Quality, Compliance & Data

DM Clinical Research; New York (NY); On-site; USD 85,000 - 120,000; Full time

Job summary

A leading clinical research organization seeks a Clinical Research Site Manager in New York City to ensure high-quality research is conducted according to FDA regulations and guidelines. The role involves supervising site staff, managing study logistics, and ensuring study objectives are met. Qualified candidates have at least 4 years of clinical research experience, strong leadership skills, and an advanced degree is preferred. Join a team that values meticulous research and fosters professional growth.

Qualifications

• At least 4 years of clinical research coordinator experience, including 2 years of management experience.
• Certified Clinical Research Coordinator (CCRC) or equivalent certification preferred.
• Solid teamwork, organizational and problem-solving skills.

Responsibilities

• Ensure quality research at investigative sites in accordance with protocols and regulations.
• Supervise site staff and ensure timely completion of training.
• Ensure preparedness for sponsor and CRO visits.
• Manage staff performance and facilitate training.

Skills

Teamwork

Organizational skills

Interpersonal skills

Problem-solving skills

Critical Thinking

Reading Comprehension

Communication skills

Multitasking

Attention to detail

Education

Advanced degree

Tools

Clinical trial management systems

Relevant software

Job description

A leading clinical research organization seeks a Clinical Research Site Manager in New York City to ensure high-quality research is conducted according to FDA regulations and guidelines. The role involves supervising site staff, managing study logistics, and ensuring study objectives are met. Qualified candidates have at least 4 years of clinical research experience, strong leadership skills, and an advanced degree is preferred. Join a team that values meticulous research and fosters professional growth.