Clinical Jobs in King of Prussia, Pennsylvania
Clinical Development Scientist needed for a contract opportunity with Yoh's client located in King of Prussia, PA. The Big Picture - Top Skills Should You Possess: - Clinical Research What You'll Be Doing: - The successful candidate will design and oversee delivery of studies in support of sponsored programs/projects in the Immuno-Inflammation therapy area. The jobholder will conduct studies in ac...
Reproductive Medicine Associates of Philadelphia is a leading infertility practice whose mission is to offer our patients the most up to date, appropriate treatment available in a caring, compassionate manner. If you are as passionate about our mission as we are, then join our remarkable team! We are looking for a RN to work in collaboration with our physician team, under the direction of our clin...
Director of Clinical Operations Hospice Grane Hospice is currently accepting candidates for the Director of Clinical Operations for our new location in King of Prussia. The successful candidate will be responsible for the implementation, delivery, coordination and supervision of Hospice services in compliance with State regulations and internal policies and procedures. Proven leadership skills, go...
CLINICAL THERAPIST Saint Gabriel's Hall (Audubon, PA), a component of Saint Gabriel's System which operates both residential and day treatment centers under the auspices of Catholic Social Services of the Archdiocese of Philadelphia, seeks a Master’s level Clinical Therapist (MSW preferred) to provide individual, group and family therapy to adjudicated male juveniles and dependent youth. Master's...
Get referred to this job Schedule: Full-time Join Accenture and help transform leading organizations and communities around the world. The sheer scale of our capabilities and client engagements and the way we collaborate, operate and deliver value provides an unparalleled opportunity to grow and advance. Choose Accenture, and make delivering innovative work part of your extraordinary career. Accen...
Requirements: - BS in Biology or Healthcare field - 1 year experience in Drug Development, Regulatory Affairs, CRA experience a plus. - Dialysis, Rheumatology, Oncology, Cardiology, Pediatrics or GI experience preferred - Ability to travel up to 80%, including overnight - Knowledge of Medical/Regulatory Terminology Description: - Assist with Administration of clinical research projects: recruiting...
RESPONSIBILITIES: Responsible for maintaining quality and ensuring that studies, documents, and submissions to federal agencies meet required industry and federally specified standards (Good Clinical Practices) Plan, schedule, and conduct internal and external quality audits including audits of clinical sites, vendors, partners, and collaborators to ensure compliance with regulations, agreements,...
Nature and Scope The Regulatory Associate provides administrative support to the Clinical Regulatory group. He/She is responsible for the organization and compilation of the regulatory submissions and maintains the regulatory files to ensure that dossiers are easily retrieved for review by the team. He/She works with pharmacovigilance to process and file Pharmacovigilance reports to the FDA in a t...
Judge Healthcare is currently seeking a Clinical Care Plan Developer to work in a virtual healthcare environment. This job will have the following responsibilities: Oversee content management strategy. Ensure that guidelines references in software demonstration content for diabetes, heart failure, COPD/asthma, and other conditions are current. Represent product in final sales presentations. Descri...
Judge Healthcare is currently seeking a Clinical Liaison for a growing Hospice organization in Montgomery County. The selected RN will have a combination of Hospice and Discharge Planning experience as well as a Marketing background. Duties include: Increase business within existing accounts as well as market to prospects. Identifies and confirms the patient plan of care for home health or hospice...
ePharmaSolutions (ePS) is a global industry-leading clinical services and technology solutions provider that supports the top pharmaceutical, biopharmaceutical and clinical research companies in the world. Our award-winning Clinical Trial Portal (CTP) and eTMF are used by more than 350,000 clinical researchers in 135 countries. At ePharmaSolutions, we welcome your knowledge, experience and enthusi...
The Clinical Solution Architect works with stakeholders, both leadership and subject matter experts, to build a holistic view of the organization's strategy, processes, information, and information technology assets. The role of the Solution Architect is to take this knowledge and ensure that the business and IT are in alignment. The Solution Architect links the business mission, strategy, and pro...
AVO MultiAmp Corporation Collegeville, 19426
Clinical Data Analyst Collegeville, PA Analyze clinical trial data, provide clinical trial analysis report with knowledge in pharmaceutical manufacturing/clinical trial using SAS/BASE, SAS/STAT, SAS/ MACRO, SAS/ GRAPH. MS in Pharmaceutical Engineering or related with related exper. Contact: HR, PI Square, Inc., 100 Springhouse Drive, #204, Collegeville, PA 19426 Source: Philadelphia Inquirer and D...
Job Details: Duration : 12+ Months Contract with possible extension Location : Collegeville, PA 19426 Title : Global Innovative Products Clinical Quality Control Reviewer The candidate will review and modify submission-ready clinical documents by demonstrating high attention to detail, in order to guarantee quality of the final document. The ability to work independently to think through results,...
Job Summary: Company: Artech Information Systems LLC Job Title: Global Innovative Products Clinical Quality Control Reviewer Location: Collegeville PA Job ID : PWR10465 Job Description: The candidate will review and modify submission-ready clinical documents by demonstrating high attention to detail, in order to guarantee quality of the final document. The ability to work independently to think th...
Global Innovative Products Clinical Quality Control Reviewer 1 year contract W2 candidates only, no subcontracting Candidate must have a BA/BS degree + 3 years experience Critical skills: Review Docs against source; Cross-tracking; attention to detail; 3+ year clinical trials knowledge; oral/written skills; QC/QA experience; Medical Writing experience. Must have at least a Bachelor's Degree POSITI...
Manages and prioritizes tasks related to data management to meet project needs. Responsible for overall quality of the database to be delivered to the statistician and sponsor. ESSENTIAL FUNCTIONS: Serve as UBC primary contact for data on a project Responsible for delivering quality databases to stakeholders and communicating any clarifications or details that would affect the data analysis to the...
This is a lead position contributing to functions of the programming roles within the Biostatistics and Programming Departments. Responsibilities include: Acts as the lead programmer on multiple studies Manages project timelines, budgets, and resources Effectively assigns and communicates priorities and work direction to ensure completion of assigned tasks on time and within budget Oversees the pr...
Company Profile: Inovio Pharmaceuticals is a Blue Bell, PA based vaccine product development company with research and engineering facilities in San Diego, CA and Blue Bell, PA. Inovio is developing a new generation of vaccines, DNA vaccines, to treat and prevent cancers and infectious diseases. These SynCon® vaccines are designed to provide broad cross-strain protection against both known and new...
Job Summary The Clinical Data Manager will act as a liaison with project managers and Data Managers at pharmaceutical companies and CROs, from protocol development to completion of a clinical drug or device development program. The core responsibility involves working with eCaseLink project managers to develop Case Report Forms, edit specifications, user acceptance testing, eCRF review and databas...
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Some questions about Clinical Laboratory Scientist as a Job?
-What kind of work do you do? Can you please describe your daily activity in sequence? -Is the job repetitive? If yes, why is it? -What kind of career path in the future is available to it? What ar...
How stable are the Clinical Research Associate jobs?
I am interested in hearing the opinions from folks who are on the field or know someone who is in the field? Are the jobs usually short contract jobs that ends with the studies? Do you have to be on t...
Clinical lab scientist question?
Hi, I'm currently a nursing student but hating the patient contact part, I also am really struggling in my classes for the past 2 semesters, and personally I feel like if I'm spending this much time s...
What kind of job can I get as a freshman to gain clinical experience?
I'm pursuing a career in clinical psychology, and I'm looking for any job that could give me experience in that field. I don't expect a big paycheck! ....Any ideas?
How to get a clinical job abroad?
Next year I'm planning on moving to Europe while trying to gain clinical hours for the Physician Assistant program. Do you have any recommendations as to how I should get started with this?
Healthcare Career Tools
Clinical Coordinator-Clinical Trials
$30,000.00 - $105,000.00
Typical Salary for Clinical Coordinator-Clinical Trials in King of Prussia
Source: Monster.com Careerbenchmarking Tool
Education / Training
Some College Coursework Completed
Source: Monster.com Careerbenchmarking Tool
Clinical Coordinator-Clinical Trials
Plans and controls clinical pharmacology studies by developing and implementing research and administrative strategies, exclusive of those actions requiring medical judgments; standardizing operating procedures across all trials; supervising staff.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Administrative Writing Skills
Health Promotion and Maintenance
Maintains patient confidence and protects operations by keeping information confidential.
Ensures clinical trials site compliance with protocol specifications, FDA, and other regulatory obligations by visiting investigative sites; conferring with site coordinators and physicians; implementing protocols; monitoring trials at sites; making recommendations as warranted to assure adherence to Federal Drug Administration and protocol guidelines; identifying potential problems and/or inconsistencies; taking action as appropriate.
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