Clinical Research Specialist: Average Salary in King Of Prussia, PA in 2024

The CR Quality Specialist C is responsible for performing GCP compliance activities for sponsored IND clinical research trials and Investigator initiated trials to verify human subjects are safe, the data accurate, complete and verifiable from source documents. The Clinical Research Quality Speciali...

The Clinical Research Data Specialist supports the data collection, analysis and reporting functions for the Office of Clinical Research (OCR) for assigned oncology trials in Phase I, II or III clinical trials and works in conjunction with a Clinical Research Nurse/Coordinator (CRN/CRC) to ensure ac...

The ACC seeks a full-time NCI/NCTN Senior Regulatory Affairs Study Start-Up Specialist to participate in the coordination of Phase I-III clinical trials sponsored by the NCI/NCTN. The NCI/NCTN Senior Regulatory Affairs Start-Up Specialist is expected to resolve, with minimal supervision, regulatory ...

The ACC One Cancer Clinical Research (OCCR) is instrumental in the development and implementation of cancer clinical trials that offer cutting-edge oncology treatments. The ACC OCCR Regulatory Affairs Office seeks a full-time Regulatory Affairs Specialist-CC to participate in the coordination of Pha...

Minimum of seven years of experience as a clinical research monitor/auditor, research nurse or research coordinator with at least three years’ experience directly monitoring/auditing or five years’ experience preparing for and fully supporting monitoring/auditing visits preferred. Additional experie...

The CR Quality Specialist C is responsible for performing GCP compliance activities for sponsored IND clinical research trials and Investigator initiated trials to verify human subjects are safe, the data accurate, complete and verifiable from source documents. The Clinical Research Quality Speciali...

The ACC seeks a full-time NCI/NCTN Senior Regulatory Affairs Study Start-Up Specialist to participate in the coordination of Phase I-III clinical trials sponsored by the NCI/NCTN. The NCI/NCTN Senior Regulatory Affairs Start-Up Specialist is expected to resolve, with minimal supervision, regulatory ...

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Initiation Clinical Research Associate. Previous experience in study set up / site initiation / study start up experience or equivalent experience in clinical research environment, with understanding of clinical trials methodology and terminology. ...

FSP (Function Service Provision)CROCRO....

The Research Associate position is an excellent opportunity for an individual who is interested in beginning a career in research, conducting unique first-in-human, Phase I clinical research trials within multiple therapeutics. The Research Associate position is a great opportunity for those with a ...

Substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Update all appropriate Clinical Trial Management Systems (CTMS) on an ongoing basis, including performing regular reviews of site level data in cli...

The Project Intake Coordinator will be responsible for receiving, reviewing and assigning new project requests within the organization. We are seeking a motivated and detail-oriented Project Intake Coordinator to join our team. The successful candidate will be responsible for assisting the project m...

The Senior Research Associate (SRA) leads, trains, and mentors a highly collaborative, interdisciplinary research and evaluation team and provides deep knowledge in specific subject areas. Trains, develops, and mentors employees' research and project skills, knowledge, and abilities; supervises proj...

Research or scholarship responsibilities may include developing both collaborative and independent research programs related to human genetics, co-supervision of postdoctoral fellows, students and other trainees, and research staff, coordinating NIH-funded grant efforts with local, national, and int...

Ensure that projects are completed on schedule following established procedures, schedules, and work plans. Coordinate the planning, organizing, control, integration, and completion of Engineering projects within area of assigned responsibility. ...

This position is responsible for fulfilling document delivery, and docket and case procurement requests using traditional and online sources (WorldCat, Lexis+, Westlaw, Bloomberg BNA, Internet, PACER, Courthouse News, and a variety of additional commercial and local providers), and other light legal...

We handle all types of commercial projects, both single-trade and multi-trade projects for the multi-site industry such as remodels, painting, fencing, etc. Maintain tracking systems for all pending, active and completed projects including but not limited to documentation uploads, status and schedul...

Research, Professor, Assistant, Technology, Education. ...

Clinical Research Coordinator A. Promote good clinical practice in the conduct of clinical investigations, including possessing and in depth knowledge of the federal regulations and guidance documents for the conduct of clinical studies and human subject protection. Coordinate the day-to-day managem...

As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...

The Clinical Research Coordinator, under the direction of the Director, CRORA and Clinical Investigators, will be responsible for the planning, implementation, and execution of Clinical Research studies in one or more departments. Prior research experience with NIH sponsored research studies, indust...

Pharmaceutical Research Associates, Inc. ...

Are you looking for an opportunity in Clinical Research?Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking Clinical Research As...

The full-time Clinical Research Coordinator will serve as the lead Coordinator on this trial alongside opportunities to participate in other research studies in the Division of Breast Surgery. Experience working with human research participants in a clinical research environment or other clinical ex...