Clinical Research Coordinator I- GYN

BILH Performance Network; Burlington (MA); On-site; USD 30,000 - 36,000; Full time

Job summary

Lahey Clinic in Burlington, MA is seeking a Clinical Research Coordinator I to support GYN studies under supervision. You will coordinate multiple trials, work with investigators and staff, and ensure protocols and regulatory requirements are followed.

The role involves screening and recruiting participants, collecting and reporting data, and traveling to national research sites as needed. Bachelor's degree and 0–2 years' experience preferred; pay range listed.

Qualifications

• Bachelor’s degree required.
• 0–2 years of experience in a research or medical setting.
• Ability to travel nationally to other research sites.
• Strong organizational, multi-tasking, and communication skills.
• Ability to work in small teams and with study participants compassionately.
• Experience with computer systems and web-based applications.

Responsibilities

• Coordinate and administer multiple research studies under supervision.
• Work with principal investigators and staff to execute trial protocols.
• Set up administrative systems to track progress of each study.
• Screen, recruit, and follow study participants and collect data.
• Report study data and ensure regulatory compliance.

Skills

Attention to detail

Organizational skills

Communication skills

Teamwork

Independent work

Problem solving

Travel willingness

Computer literacy

Experience with web-based applications

Education

Bachelor’s degree

Tools

Web-based applications

Job description

# Clinical Research Coordinator I- GYNBURLINGTON, MA • Lahey Clinic • Full-time • DayShare job:Apply now**When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives.**Under general supervision and direction will be responsible for the coordination and administration of multiple research studies. Works closely with principal investigators and research staff facilitating all aspects of assigned clinical trials. Implements study protocols in accordance to regulatory and institutional requirements. Sets up administrative systems to manage the progress of each study while screening, recruiting and following study participants and collecting and reporting study data. Interacts with study participants diagnosed with various medical conditions and diagnoses.**Job Description:****Minimum Qualifications:****Education:**Bachelor’s degree required.Licensure, Certification & Registration:None required.**Experience:**0-2 years of experience in a research or medical setting. Skills, Knowledge & Abilities:* Ability to address problems that are routine, somewhat repetitive and generally solved by following clear directions and procedures;* Ability to travel nationally to other research sites, attend investigator meetings and educational conferences as required;* Strong organizational, multi-tasking, attention to detail and communication skills;* Ability to take direction, set priorities and work somewhat independently;* Ability to demonstrate a positive attitude and respond to request in a timely and respectful manner;* Ability to work in small teams, interact with professional personnel at all levels of an organization, and work with study participants of various diseases compassionately and respectfully;* Experience with computer systems, including web-based applications;* In the absence of any of these skills, demonstrates the ability to be thoroughly trained to meet organizational standards.**Pay Range:**$21.64 – $26.50The pay range listed for this position is the base hourly wage range the organization reasonably and in good faith expects to pay for this position at this time. Actual compensation is determined based on several factors, that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other applicable factors permissible by law. Compensation may exceed the base hourly rate depending on shift differentials, call pay, premium pay, overtime pay, and other additional pay practices, as applicable to the position and in accordance with the law.## As a health care organization, we have a responsibility to do everything in our power to care for and protect our patients, our colleagues and our communities. Beth Israel Lahey Health requires that all staff be vaccinated against influenza (flu) as a condition of employment.## More than 35,000 people working together. Nurses, doctors, technicians, therapists, researchers, teachers and more, making a difference in patients' lives. Your skill and compassion can make us even stronger.## Equal Opportunity Employer/Veterans/Disabled### **Job details*** **Employment:** Full-time* **Hours/Week:** 40* **Shift:** Day* **Category:** Medical/Clinical Research* **Pay Range:** $21.64 - $26.50* **FLSA:** Non-Exempt* **Req ID:** JR102437