Job Market Guide: Research Coordinator jobs in Wilkes Barre-Scranton

Competition
Desired Skills
Years of Experience
Years of Experience distribution graph for Research Coordinators in Wilkes Barre-Scranton. Research Coordinators in Wilkes Barre-Scranton have between ${} and ${} years of experience, averaging $${} years of experience.

16 Research Coordinator jobs in Wilkes Barre-Scranton

Research Coordinator

Hyde Park, NY
The Research Coordinator will assist with day to day operations of CDC and CDPH funded projects that involve providing social service support to individuals living with or at risk for HIV/STIs in South Chicago.
industry
Business Services
experience
Less than 5 years

Research Coordinator

New York, NY
In this role, you will implement study data collection and intervention protocols.
industry
Education
experience
Less than 5 years

Research Coordinator

New York, NY
The Research Coordinator will manage and oversee research project activities ensuring adequate recruitment, data collection quality and integrity, and full compliance with all regulatory guidelines. Manages professional and support staff, reviewing work product to ensure study protocol is followed as written and approved by the relevant IRB..
industry
Education
experience
Less than 5 years

Research Coordinator

New York, NY
In this role, you will provide professional phone coverage at all times; screen all calls and determine through independent judgment those which require immediate attention.
industry
New Media
experience
Not Specified

Research Coordinator

New York, NY
The Research Coordinator is an entry-level role for candidates with research experience and who have a bachelors degree in behavioral or quantitative social sciences or a related subject. You will work as part of a team responsible for delivering insights and ad effectiveness measurement.
industry
Information Services
experience
Less than 5 years

Hyde Park, NY
In this role, you will be responsible for the oversight/monitoring of all clinical trial expenses; reviews the protocol plan to differentiate standard of care versus research to ensure that clinical care expenses, personnel effort, site initiation costs, IRB fees, pharmacy costs, equipment, and supplies are tracked and captured as direct costs to the clinical trial.
industry
Business Services
experience
Less than 5 years

Ridgewood, NJ
In this role, you will coordinates and administers research study associated activities under the direction of the Principal Investigator (PI) and Research Nurse Manager/Supervisor. Assists in project planning; coordinates and implements clinical research.
industry
Patient Care
experience
11 - 15 years

New York, NY
In this role, you will be responsible for recruiting, consenting and interviewing post-Acute Coronary Syndrome patients and/or stroke patients in both the Emergency Department and inpatient settings; administering standardized questionnaires - some with potentially sensitive questions about mood; conducting follow-up interviews or sub-study visits on-site or in the community.
industry
Education
experience
Less than 5 years

New York, NY
In this role, you will maintain appropriate documentation associated with the assigned clinical study.
industry
Healthcare IT
experience
Less than 5 years

Hyde Park, NY
The Research Coordinator will provide technical and administrative support for the Program in Oral Health, Systemic Health, Well-Being and the Social Sciences.
industry
Business Services
experience
Not Specified

Research Coordinator

New York, NY
The research coordinator will work with the principal investigator ( PI ) in the department of epidemiology and population health at the albert einstein college of medicine.
industry
Education
experience
Less than 5 years

New York, NY
In this role, the selected candidate will deliver drug products to study areas, interact with co-workers, study coordinators, investigators, sponsors and hospital staff.
industry
Education
experience
Less than 5 years

New York, NY
In this role, you will coordinate recruitment, participant enrollment, and clinical services. Assesses patient eligibility for inclusion in clinical trials (may be multiple or various PIs). Ensures proper consent protocols have been followed for study participation.
industry
Education
experience
Less than 5 years

$42K - $60K - New Brunswick, NJ
In this role, you will be responsible for assisting the clinical research team in overall study coordination, including, but not limited to, preparing for study initiation and activation, acquisition of source documents, record maintenance, preparing study documents, patient registration, coordinating and data entry.
industry
Education
experience
Less than 5 years