Job Market Guide: Research Coordinator jobs in Philadelphia

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

36 Research Coordinator jobs in Philadelphia

Newark, DE
In this role, you will plan, implement and evaluates protocol-related care of participants and data for select projects.
industry
Patient Care
experience
Less than 5 years

$50K - $72K - New Brunswick, NJ
In this role, you will provide guidance and updates on regulatory requirements and IRB submissions to the project teams, Nurse Coordinators and Director.
industry
Education
experience
Less than 5 years

$50K - $72K - New Brunswick, NJ
In this role, the selected candidate will be responsible to manages the regulatory activities of the clinical research center.
industry
Education
experience
Not Specified

$80K - $100K - Newark, DE
The candidate must have on-site clinical monitoring experience including source data verification using medical charts, review of regulatory study binders, adverse events and data clarification process.
industry
Health & Beauty
experience
Not Specified

$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
Not Specified

$45K - $68K - New Brunswick, NJ
In this role, you will assist in the maintenance and update of the GIS database, including updating existing datasets and creating new data.
industry
Education
experience
Less than 5 years

New York, NY
In this role, you will be responsible for regulatory oversight, data collection, quality control and data analysis for research projects, databases, and research protocols.
industry
Patient Care
experience
Less than 5 years

Manhasset, NY
In this role, you will conduct patient interviews, explains policies and procedures to patient/significant others, reviews the patient's chart and answers questions correctly and courteously. The selected candidate will be adhering to protocol; performs the administration of the agent, electrocardiograms, IV placement, phlebotomy, specimen collection, vitals, patient and adverse event assessment.
industry
Healthcare IT
experience
Not Specified

Baltimore, MD
In this role, you will be responsible for monitoring the clinical course and collection of research data on patients entered onto research protocols at the Sidney Kimmel Comprehensive Cancer Center and possibly, external institutions.
industry
Education
experience
Less than 5 years

Baltimore, MD
In this role, you will be responsible for monitoring clinical course and collection of research data on patients entered onto research protocols in the Neurosurgery Pain Institute Clinical Trials Group and possibly, external institutions.
industry
Education
experience
Not Specified

Baltimore, MD
In this role, you will work closely with faculty to develop, evaluate and implement policy and procedures that will be part of the official Policy and Procedure manual for the study.
industry
Education
experience
Not Specified

Research Coordinator

New York, NY
In this role, the selected candidate will support all study activities with accountability and follow-through. Communicates effectively, in writing, by phone, and in person, with faculty, medical and research staff, sponsors, and institutional offices.
industry
Business Services
experience
Less than 5 years

Baltimore, MD
In this role, the selected candidate will ensure that the divisions research projects and related activities are performed in accordance with institutional and external policies and procedures.
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
Not Specified

Research Coordinator

New York, NY
In this role, you will develop and maintains research databases; performs primary data entry into research databases; performs secondary data analyses and data checks.
industry
Education
experience
Less than 5 years

New York, NY
In this role, you will develop and manage a system so that all relevant documents and materials related to all projects are organized and stored for easy access and facilitate and support communication and process flow across relevant teams and people for each project.
industry
New Media
experience
Not Specified

Baltimore, MD
In this role, you will be responsible for monitoring the clinical course and collection of research data on patients entered onto research protocols at the Sidney Kimmel Comprehensive Cancer Center and possibly, external institutions.
industry
Education
experience
Not Specified

New York, NY
The candidate will collect data and complete case report forms for all study visits as required by the protocol and consistent with GCP, HIPAA FDA/HHS, state and institutional regulations.
industry
Education
experience
Less than 5 years

New Brunswick, NJ
In this role, you will be responsible for the supervision of day-to-day clinical research operations and communication of priority services that will support and enable the growth of clinical research, particularly in the areas of recruitment, retention, coordination of research procedures and data management.
industry
Education
experience
Not Specified

Research Coordinator

New York, NY
In this role, you will conduct literature reviews, which will involve searching the literature within a targeted domain, applying critical appraisal to the findings, and synthesizing results.
industry
Education
experience
Not Specified

Baltimore, MD
In this role, you will assist the principal investigator and/or program manager in defining information and plans required to accomplish goals of studies. May help design and create protocol specific data collection forms with assistance.
industry
Education
experience
Not Specified

$42K - $60K - New Brunswick, NJ
In this role, the selected candidate 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
Not Specified

Hershey, PA
In this role, you will be responsible for implementation of clinical research protocols under physician investigator guidance and delegation and clinical research specialist and/or clinical research coordinator II guidance.
industry
Misc. Healthcare
experience
Less than 5 years

$46K - $70K - New Brunswick, NJ
In this role, the selected candidate will promote and supports the assigned tasks from the Rutgers University Center for Ocean Observing Leadership.
industry
Education
experience
Less than 5 years