Job Market Guide: Clinical Manager jobs in Philadelphia

Competition
Low
0.195939
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Clinical Managers in Philadelphia. Clinical Managers in Philadelphia have between ${} and ${} years of experience, averaging $${} years of experience.

53 Clinical Manager jobs in Philadelphia

Philadelphia, PA
Develop and maintain a close liaison with project client contacts, core team members, and Project Managers to drive the data management aspects of project delivery.
industry
Biotech/Pharma
experience
5 - 7 years

Philadelphia, PA
Conducting reviews of system set-ups and documents to ensure high quality of deliverables in accordance with quality standards and SOPs.
industry
Advertising & Marketing Services
experience
5 - 7 years

Princeton, NJ
Develop and maintain a close liaison with project client contacts, core team members, and Project Managers to drive the data management aspects of project delivery.
industry
Biotech/Pharma
experience
5 - 7 years

Towson, MD
This position provides technology assessments, purchasing assistance, and equipment safety and life cycle management.
industry
Misc. Healthcare
experience
5 - 7 years

New York, NY
Promotes a positive and professional image for pharmacy by advocating and demonstrating exemplary teamwork and leadership; participates and acts as the inter and intra department liaison in collaborations with nursing, ancillary department directors and medical staff.
industry
Patient Care
experience
Not Specified

Plymouth Meeting, PA
Develops and manages clinical protocols and amendments, informed consent forms, training material, case report forms, diary cards, clinical study reports and other clinical documents, and contributes to the development of investigator's brochures.
industry
Biotech/Pharma
experience
5 - 7 years

Mgr Clinical Services

New York, NY
Responsible for oversight of day-to-day operations of the Clinical Utilization Management Department staff.
industry
Patient Care
experience
5 - 7 years

Wilmington, DE
Collaborates with internal departments to support and develop standard operating procedures/working practices/collection forms and adheres to company and departmental SOPs as required.
industry
Biotech/Pharma
experience
5 - 7 years

Princeton, NJ
Prepare and actively participate as operational lead in internal project review meetings. Depending on size and scope of project, this job duty may be performed in collaboration with a Project Director.
industry
Biotech/Pharma
experience
5 - 7 years

Princeton, NJ
Work with staff in Project Management, Clinical Trial Design & Strategy, Vendor Management, Regulatory Affairs, Quality Assurance, Business Development and Operations, to provide relevant clinical and ancillary supply data critical to the ability of the organization to develop plans for the successful implementation and conduct of global clinical trials.
industry
Biotech/Pharma
experience
8 - 10 years

Hampton, NJ
This individual will also be responsible for daily monitoring and management of the supply chain for company sponsored clinical studies as well as relevant investigator initiated studies, including monitoring supply levels using IXRS systems.
industry
Biotech/Pharma
experience
Less than 5 years

Allendale, NJ
Supervise the implementation of clinical programs and track their progress. Oversee the planning of new clinical programs and the development of clinical protocols
industry
Medical Devices & Diagnostics
experience
5 - 7 years

Brooklyn, NY
Manages the day-to-day operations of Clinical Support Team to ensure effective and quality service delivery.
industry
Misc. Healthcare
experience
5 - 7 years

Easton, MD
Directs and supervises the functions of coding, abstracting, data collection and computer entry into MEDITECH or other data systems for SRH.
industry
Misc. Healthcare
experience
5 - 7 years

Philadelphia, PA
The incumbent will initiate, review, negotiate and process clinical research budgets and contracts for Temple Health system.
industry
Business Services
experience
5 - 7 years

Philadelphia, PA
Providing guidance in establishment of screening and enrollment procedures using the electronic health record system.
industry
Business Services
experience
5 - 7 years

Collegeville, PA
Responsible for ensuring that Clinical Study Support staff and eTMF supports staff share best practices and serve as a change agents for company both internally and externally.
industry
Biotech/Pharma
experience
5 - 7 years

Edison, NJ
Coordinate and liaise with Daiichi Sankyo QA on audit activities Provide oversight of the transmittal of trial and site level documents to the Daiichi Sankyo Document Control Center (DCC) in support of the Trial master File (TMF).
industry
Business Services
experience
5 - 7 years

Raritan, NJ
Monitor team member ICSR quality and compliance, with an emphasis on SUSARs accuracy, completeness (e.g. case narratives, coding activities, AOSE, etc.) to maintain regulatory compliance and strong partnerships with stakeholders (GCO).
industry
Biotech/Pharma
experience
5 - 7 years

New York, NY
Responsible for assembling project plans and teamwork assignments, directing and monitoring work efforts on a daily basis, identifying resource needs, performing quality review; and escalating functional, quality, timeline issues appropriately.
industry
Patient Care
experience
8 - 10 years

Bridgewater, NJ
The CTOM is responsible for the overall operational planning and activities for the implementation and conduct of studies (clinical trials, observational studies, compassionate use and registries) including oversight of data management activities in compliance with GCPs, SOPs and standards within established timelines and budgets.
industry
Consulting
experience
8 - 10 years