Job Market Guide: Clinical Research Coordinator jobs in Salisbury

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

36 Clinical Research Coordinator jobs in Salisbury

Arlington, VA
In this role, you will be ability to independently organize and manage multiple complex tasks simultaneously.
industry
Consulting
experience
Less than 5 years

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

Alexandria, VA
In this role, you will manage data requests to entities regarding programs, projects, budgets, and progress.
industry
Business Services
experience
5 - 7 years

Arlington, VA
In this role, the successful candidate will assist clients with the technical and programmatic management of a portfolio of research and development (R&D) efforts.
industry
Consulting
experience
Less than 5 years

Silver Spring, MD
In this role, the selected candidate serves as a liaison for collaborating institutions, human subjects review boards, and commercial partners; provides guidance or assistance on participant screening, consent, data collection and storage.
industry
Telecommunications
experience
5 - 7 years

Washington, DC
The Coordinator, Research & Prospect Management will work in the Research & Prospect Management office under the direction of the Director of Research & Prospect Management and will have the primary responsibility of identifying prospective donors and collecting, evaluating, analyzing, organizing, packaging, and disseminating detailed prospect research on current and potential prospects for the Office of Development and Alumni Relations.
industry
Education
experience
Less than 5 years

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

Falls Church, VA
In this role, you will be responsible for clinical trials and outcomes research directly to patients, optimizing individual health and well-being.
industry
Healthcare IT
experience
Less than 5 years

Washington, DC
In this role, the selected candidate will support the goals of the Gen Med organization by initiating, monitoring, and closing out clinical study sites following GCP and ICH guidelines as well as Novartis SOPs and ensuring that study milestones are met.
industry
Biotech/Pharma
experience
8 - 10 years

Arlington, VA
In this role, you will assist clients with the technical and programmatic management of a portfolio of research and development (R&D) efforts. Serve as a coordinator responsible for managing technical scope, budget, and schedule of multiple projects.
industry
Consulting
experience
Less than 5 years

$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

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

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

Alexandria, VA
In this role, the selected candidate will coordinate financial aspects of study implementation and management from protocol feasibility through study close-out per company Research Center and Research Department policies and guidelines.
industry
Healthcare IT
experience
Less than 5 years

Columbia, MD
In this role, the selected candidate will help patients improve their quality of life by delivering outstanding clinical outcomes in a chronic hemodialysis setting.
industry
Misc. Healthcare
experience
Not Specified

Silver Spring, MD
In this role, you will selects and observes subjects and assists with data analysis and reporting.
industry
Telecommunications
experience
Less than 5 years

Baltimore, MD
In this role, you will be responsible for the Inflammatory Clinical Coordinator include patient and team member education, clinical patient assessments, and longitudinal patient management.
industry
Healthcare IT
experience
Not Specified

Silver Spring, MD
In this role, you will be responsible for coordinating and assuring integrity of all activities associated with conducting a clinical trial that involves multiple DoD and VA sites.
industry
Telecommunications
experience
5 - 7 years

Alexandria, VA
In this role, you will direct and oversee Clinical Development/Operations and Regulatory Affairs process for a research and development services provider conducting clinical trials of experimental vaccines and biologics.
industry
Business Services
experience
11 - 15 years

Baltimore, MD
In this role, you will provide direction and support to unit staff. Supervises admissions, conducts assessment of patient's needs, and initiates nursing care plans. Evaluates and documents patient progress.
industry
Healthcare IT
experience
Not Specified

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

Silver Spring, MD
In this role, you will be responsible for provides assurance of accurate documentation in compliance with all governing regulations.Develop databases or modify existing databases to create datasets for analysis.
industry
Telecommunications
experience
5 - 7 years

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

Silver Spring, MD
S/he is responsible for coordinating and assuring integrity of all activities associated with conducting a clinical trial that involves multiple DoD and VA sites. S/he will ensure compliance with all local, state, federal, and international regulatory requirements.
industry
Telecommunications
experience
5 - 7 years