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.

47 Clinical Research Coordinator jobs in Wilkes Barre-Scranton

South Plainfield, NJ
The Clinical Trial Coordinator (CTC) is responsible for providing in-house support and assistance to assigned study teams and GTMM.
industry
Biotech/Pharma
experience
Less than 5 years

Pearl River, NY
Responsible for review of subject level data across a study and for coordinating with the Lead Clinician for study level review as delegated.
industry
Biotech/Pharma
experience
Less than 5 years

Clinical Coordinator

New York, NY
The Coordinator provides essential clinical leadership for these Centers and directly supervises the clinical support staff (RNs, LPNs, and MAs), including hiring, on boarding, scheduling, and performance management.
industry
Education
experience
5 - 7 years

Morristown, NJ
The Clinical Trial Coordinator (CTC) is responsible for providing in-house support and assistance to assigned study teams and GTMM.
industry
Biotech/Pharma
experience
Less than 5 years

Collegeville, PA
Responsible for review of subject level data across a study and for coordinating with the Lead Clinician for study level review as delegated.
industry
Biotech/Pharma
experience
Less than 5 years

Edison, NJ
Authoring of Clinical Study Subject Narratives for assigned studies, Review work of other writers (in-house or consultant) for accuracy, quality, focus, and adherence to format and stylistic requirements, review data to determine the appropriate tabular and textual formats, and the clarity, logic and order of presentation.
industry
Biotech/Pharma
experience
11 - 15 years

$120K -. $130K - Madison, NJ
Knowledge of drug development (all clinical research process including protocol and case report form design, etc) .
industry
Biotech/Pharma
experience
5 - 7 years

New York, NY
Researches and communicates pertinent scientific/clinical information regarding clinical trials that Novella Clinical is requested to conduct feasibility on, or bid on in proposal form.
industry
Biotech/Pharma
experience
Less than 5 years

New York, NY
Verify and ensure the accuracy, completeness, specificity and appropriateness of diagnosis codes based on services rendered.
industry
Healthcare IT
experience
Less than 5 years

Woodcliff Lake, NJ
Ensure the training of CROs/investigators on protocol, regulatory, Eisai SOPs and data issues. Reviews and approves monitoring reports and ensures tracking of ongoing site issues.
industry
Security Services
experience
Less than 5 years

Hershey, PA
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

Research Coordinator

New York, NY
Responsible for the timely submission of initial and continued Einstein IRB, BRANY IRB and Central Protocol and Data Management Unit (CPDMU) approval for our site and collaborating institution sites.
industry
Market Research
experience
Less than 5 years

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 Brunswick, NJ
Provides benchmarking, analysis and modeling assistance, and recommendations for targeted enrollment growth initiatives (e.g., international, out-of-state, multicultural, merit scholars) in coordination with appropriate staff.
industry
Education
experience
Not Specified

Clinical Scientist

New Providence, NJ
The Clinical Scientist serves a medical research function and applies a broad knowledge of clinical research activity, therapeutic area knowledge and regulatory requirements to facilitate the development and implementation of clinical studies.
industry
Industrial Equipment & Supply
experience
Less than 5 years

Coatesville, PA
Responsible for overseeing the daily operations of an assigned unit or clinic section within a hospital.
industry
Healthcare IT
experience
Less than 5 years

New York, NY
The Clinical Care Coordinator will adopt ColumbiaDoctors' care coordination process and workflow to achieve improved health of populations.
industry
Education
experience
5 - 7 years

New York, NY
Processing of chemotherapy orders according to protocol/safety guidelines, assessing, teaching, and monitoring of chemo patients, conducting pharmacokinetic studies and administering conventional and investigational drugs via peripheral, central , and special routes.
industry
Patient Care
experience
Less than 5 years

Princeton, NJ
Collaborate with multifunctional teams to develop scientifically sound testing strategies, timelines and data to meet project goals and timing.
industry
Business Services
experience
Less than 5 years

Cranbury, NJ
The Clinical Research Associate is responsible for assisting the Clinical Operations team(s) in overseeing sites conduct of clinical studies through monitoring and efficiently and effectively communicating site related items to the study team.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

Clinical Scientist

$50K - $60K - Pearl River, NY
In this role, you will act as Clinical Scientist.
industry
Biotech/Pharma
experience
Less than 5 years

Research Coordinator

Danville, PA
Provide educational content regarding the rationale, importance and potential for involvement to patients.
industry
Healthcare IT
experience
Not Specified

New York, NY
Develop, review, negotiate and approve all clinical research budgets associated with any non-exempt IRB/Privacy Board protocols Information Management & Training Support.
industry
Patient Care
experience
5 - 7 years

Jersey City, NJ
Responsible for collection, dissemination, and/or tracking of regulatory documents as required; maintains accurate tracking and reporting of study management data.
industry
Biotech/Pharma
experience
Less than 5 years