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

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

52 Clinical Research Coordinator jobs in Wilkes Barre-Scranton

Titusville, NJ
The Clinical Pack & Label (P & L) Outsourcing Coordinator will be responsible for the day to day management of their outsourced packaging and labelling orders.
industry
Security Services
experience
Less than 5 years

New York, NY
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

New York, NY
In this role, you will be responsible for developing and monitors the hospitals policies/procedures regarding utilization of medications in collaboration with the medical staff, Pharmacy, and Therapeutics Committee.
industry
Healthcare IT
experience
Less than 5 years

New York, NY
In this role, you will be responsible to participate in an individualized training or orientation program geared to teaching or reinforcing the principles of Clinical Nursing Research.
industry
Patient Care
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

New York, NY
In this role, you will maintain appropriate documentation associated with the assigned clinical study.
industry
Healthcare IT
experience
Not Specified

New York, NY
In this role, the selected candidate will collaborate with designated physicians and research team members (consisting of the principle investigators, Research Study Assistants, Data Managers and Nursing Staff) to develop and conduct clinical trials.
industry
Healthcare IT
experience
Less than 5 years

New York, NY
The Cognitive Software Developer, works under the direction of Dr. James K. Min, Director of the Dalio Institute of Cardiovascular Imaging (ICI), and is a member of Divisions machine learning and artificial intelligence development and implementation team.
industry
Business Services
experience
Less than 5 years

New York, NY
In the role of Clinical Pharmacy Coordinator, you will implement, coordinate and evaluate all clinical Pharmacy services, including JCAHO standards.You will also assist and direct MUEs (Medication Usage Evaluations), collaborate with the medical staff, and establishe criteria for the safe, effective and appropriate use of medication.
industry
Healthcare IT
experience
Less than 5 years

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

$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

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

$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

Tarrytown, NY
In this role, the selected candidate will collaborate with the Regulatory Team to provide PK/PD data in support of regulatory documents, communications, meetings and presentations as needed.
industry
Biotech/Pharma
experience
Less than 5 years

$60K - $90K - Plymouth Meeting, PA
In this role, the selected candidate will assist in the preparation of IRB and Ethics committee submissions; Managing and developing Clinical Studies, Write Papers, and Clinical Protocols.
industry
Biotech/Pharma
experience
Not Specified

New York, NY
The primary goal for this position is to produce measurable improvements in dialysis patient outcomes by building on a solid foundation of clinical research.
industry
Healthcare IT
experience
Less than 5 years

New York, NY
In this role, you will implement the standards for research protocols in compliance with regulatory, institutional and external agencies.
industry
Patient Care
experience
Not Specified

King Of Prussia, PA
The Clinical Safety Scientist will support Clinical Safety Physicians in the safety review process and evaluation of safety data throughout the product lifecycle using a combination of quantitative and qualitative approaches.
industry
Engineering Services
experience
Not Specified

New York, NY
In this role, you will investigate the clinical significance of variants found in sequencing-based assays search online mutation databases and published literature.
industry
Biotech/Pharma
experience
Less than 5 years

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 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

$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

$100K - $140K - Woodcliff Lake, NJ
In this role, the selected candidate will prepare and review project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of registration dossier documents (ISS, ISE, Investigator Brochure, etc.).
industry
Biotech/Pharma
experience
5 - 7 years

New York, NY
In the role of Clinical Pharmacy Coordinator, you will implement, coordinate and evaluate all clinical Pharmacy services, including JCAHO standards. You will also assist and direct MUEs (Medication Usage Evaluations), collaborate with the medical staff, and establishe criteria for the safe, effective and appropriate use of medication.
industry
Healthcare IT
experience
Less than 5 years