Clinical Research Study Coordinator

Southgate Medical Group, LLP; New York (NY); On-site; USD 54,000 - 84,000; Full time

Benefits offered by this job

401k with match

Free skin center services

Scrubs provided

Paid time off

Paid holidays

Life insurance

Disability insurance

Health insurance with HSA

Bonuses

Flexible schedule

Job summary

Southgate Medical Group, LLP is seeking a Clinical Research Study Coordinator to join our research team in a flexible full/part-time role. The position involves running trials, ensuring protocol compliance, and coordinating participant care in a fast-paced setting.

Responsibilities include obtaining informed consent, data collection, patient monitoring, and collaboration with investigators and sponsors. A competitive benefits package accompanies the role, with opportunities for bonuses based on

Qualifications

• Familiar with research regulations and patient care in research settings.
• Ability to use computers and electronic applications for study tasks.
• Experience drawing blood for research samples.
• Develop screening and recruitment materials for trials.
• Capable of working in a multidisciplinary team.
• Good physical condition and stamina.

Responsibilities

• Run clinical trials for multiple protocols across diseases.
• Perform tasks to deliver safe, high-quality care for participants and sponsors.
• Understand and implement clinical trial protocols.
• Complete required research certifications.
• Administer informed consent as delegated by PI.
• Follow up on abnormal test results with patient calls.
• Develop and maintain study source documentation.
• Administer injections, ECGs and CGMs as prescribed.

Skills

Regulatory compliance

Computer & data systems

Blood collection

Recruitment materials

Multidisciplinary teamwork

Stamina

Job description

Job Description

Full time or Part time

Join our outstanding team of professionals. We are looking for a Clinical Research Study Coordinator to work as part of our research team. We provide 401k with match, free skin center services, scrubs, generous paid time off, 6 paid holidays, life insurance, long and short-term disability insurance and partial payment of health, dental and vision insurance with a Health Savings account and periodic bonuses. FLEXIBLE SCHEDULE and NO MAJOR HOLIDAYS!

Responsibilities:

• Running clinical trials for various protocols with a diverse set of disease entities.
• Complete necessary tasks to effectively and efficiently provide safe, quality care in order to facilitate optimal clinical research trial outcomes for research participants and sponsors
• Understanding and implementing clinical protocols
• Undertaking all necessary research certification courses (provided by site and sponsor)
• Administering informed consent as delegated by Principle Investigator
• Problem-solving, call patients on abnormal test results
• Development and utilization of study source documentation
• Administer prescribed medications injections, ECGs, CGM's

Skills:

• Knowledge and or capability to adhere to research regulations, and procedures to administer relevant research related patient care.
• Knowledge of computer and electronic applications.
• Collection of blood samples
• Development of screening and recruitment materials
• Ability to undertake a variety of diverse care tasks and work in a multidisciplinary team
• Good physical condition and stamina

Job Type: Full Time or Part time

Pay: $54,000-$84,000 per year based on license and qualifications and research experience

Related keywords: LPN, RN, registered nurse, nurse, research, research coordinator, nurse rn, research nurse

research

Company Description

We are a practice that knows that integrity is the key to our success. Without a doubt, we have the highest quality of providers and staff.