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19 days old

Clinical Study Coordinator

Kelly Services
Danbury, CT 06813
**Clinical Research Study Coordinator**



Remote



1 year contract / Part-time





**Summary:** The Clinical Research Study Coordinator will work collaboratively with the Associate Director of Research Programs to implement virtual clinical research studies. This is a part time, 20 hour per week position expected to last 12 months.



**Responsibilities:**




+ Accountable for the successful execution of a research study, with virtual clinical assessments, through all phases of the study: planning, enrollment, engagement, retention, and close out

+ Responsible for performing research operations in accordance with the study protocol and working in partnership with the Associate Director of Research to coordinate research activities.

+ Develop a manual of procedures and standard operating procedures, including virtual clinical study visit and assessment protocols with the standards customary in the clinical research industry.

+ Conduct active outreach to deliver or exceed project enrollment targets, establishing rapport with study participants.

+ Schedule and conduct 4-5 virtual study visits with each participant, including virtual clinical endpoint assessments, over a 12-month period and conducting ongoing follow-up with families as needed.

+ Be responsible for accurate and timely data entry into the electronic research study system.

+ Develop weekly written project updates and participate in weekly project meetings with NORD research team.

+ Demonstrate compliance with good clinical practice (GCP) and applicable law.

+ Understand and promote compliance with all applicable healthcare and research regulations.

+ Perform other duties and functions as assigned.



**Qualifications:**




+ Bachelors degree in Nursing or a related field required;

+ Licensed clinical practitioner with specialty in pediatric populations is required;

+ At least 5 years of clinical research experience required;

+ Experience working with rare disease families preferred;

+ Experience with developing study protocol procedure documentation required.

+ Excellent verbal and written communication skills;

+ Superior attention to detail, organization, planning, and time management skills;

+ Independent self-starter with a strong desire to contribute and achieve tangible results;

+ Demonstrable empathy for people with rare diseases;

+ Interest in joining a dedicated, highly-motivated team that works collaboratively and creatively!




**Why Kelly** **** **?**



Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interestsits the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.




**About Kelly** ****



At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/non-traditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.


Kelly is an equal opportunity employer committed to employing a diverse workforce and providing accommodations for people with disabilities in all parts of the hiring process as required under its Employment Accommodation Policy. Kelly will work with applicants to meet accommodation needs that are made known to Kelly in advance.

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Posted: 2020-10-09 Expires: 2020-11-09

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Clinical Study Coordinator

Kelly Services
Danbury, CT 06813

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