Clinical Research Specialist: salario promedio en 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 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 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 ...

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...

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 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 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...

Substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. ...

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SOP(Standard Operating Procedure).SDV: Source Data Verification).IRB (Institutional Review Board)....

JobPosting","title":"PMOGA Community & Market Coordinator","datePosted":"2024-06-26T00:00:00","validThrough":null,"description":"How will you make a difference to PMI?\nThe PMOGA Community and Market Coordinator is integral in providing operational and administrative support to both the PMOGA Commun...

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...

Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ens...

This scientist will work closely with team members and will primarily be responsible for conjugation, purification, and analytical characterization of these molecules. ...

Our client, a world-leading Pharmaceutical Company in Spring House, PA is currently looking for a Bioconjugation Scientist to join their expanding team. Job Title: Bioconjugation Scientist / Protein Purification. This scientist will work closely with team members and will primarily be responsible fo...

He or she will perform a preliminary protocol assessment with the Supply Chain Lead (SCL), Clinical Research Pharmacist (CRP) and clinical team members (e. IRT strategy for clinical customer, investigator site, Global Clinical Supply, and ultimately for the patient. Job Title: Interactive Response T...

Clinical Research Coordinator in Media, PA (19063). Bachelor's Degree; 1+ Years of Clinical Research Coordinating experience. ...

We are looking for an experienced Research Scientist to join an exciting and rapidly growing immunology/immuno-oncology startup company in Philadelphia, PA! Prospective candidates must have oncology and/or immunology drug discovery experience and immunology assays experience (cytotoxicity, MSD, etc)...

We are seeking a highly motivated Senior Research Associate to join our Oncology Research team. ...

This position will require the candidate to lead a small team of scientists in the Oncology large molecule discovery setting from target validation through IND enabling studies to support First-in-Human (FIH) clinical studies. ...

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...

The RA II supports and may manage Research Assistants and Research Associate I staff and works alongside Research Associate III and Senior Research Associate staff in conducting statistical tasks (e. The Research Associate II (RA II) conducts data analysis supporting complex research and evaluation...

Provide support and management of a sponsored research portfolio. Manage fiscal and administrative aspects of federal and non-federal research grants. ...

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. ...