Clinical Research Coordinator

The Dermatology Specialists; New York (NY); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading dermatology practice in New York City is seeking a dedicated Research Assistant to join their Clinical Research team. The position offers a full-time schedule and provides opportunities for career advancement within the healthcare sector, alongside a comprehensive benefits package.

Benefits

Opportunities for career growth

Benefits package (medical, dental, vision)

56 hours of paid time off

401(k) plan

Qualifications

• Experience in clinical trials as a Research Assistant.
• Knowledge of phlebotomy.
• Ability to conduct protocol procedures such as interviewing subjects and obtaining informed consent.

Responsibilities

• Conduct protocol procedures such as data collection and educating participants.
• Work with Principal Investigators and manage data entry.

Skills

Communication

Organizational Skills

Time Management

Attention to Detail

Flexibility

Multitasking

Job description

New York City's Largest Dermatology Practice

We're a full-service dermatology practice with 50+ locations across Manhattan, Brooklyn, Queens, Long Island, Delaware, and Philadelphia.

Are you passionate about clinical research and patient care? Do you have strong communication and medical research skills but haven't had the opportunity to apply them? Are you looking to become a dermatologic expert in cosmetic and medical treatments? This is an excellent opportunity to advance your career in healthcare.

We are the fastest growing dermatology practice with 41 locations across four New York City boroughs and expanding. We are seeking a friendly, driven, and hardworking individual to join our Clinical Research team.

This is a full-time position, with working hours from Tuesday to Friday, 10:00 AM to 7:00 PM (schedule may be adjusted based on discussions).

What We Are Looking For

• Experience in clinical trials as a Research Assistant
• Knowledge of phlebotomy
• Proficiency in EDC entry and medical intake processes
• Experience with IRB submissions
• Excellent communication and organizational skills
• Ability to conduct protocol procedures such as interviewing subjects, data collection, obtaining informed consent, and educating participants about study criteria
• Experience working with Principal Investigators
• Strong time management and innovative skills
• Detail-oriented team player with flexibility
• Ability to multitask in fast-paced environments
• Availability for evenings and weekends (preferred but not required)

Compensation and Benefits

• Hourly Range: $26 - $28/hr
• Opportunities for career growth
• Benefits package (medical, dental, vision)
• 56 hours of paid time off (sick, personal, vacation)
• 401(k) plan