Clinical Jobs in Pottstown, Pennsylvania
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...
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,...
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...
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...
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...
Company Background TELA Bio, Inc. is a venture-backed medical device company located in Malvern, Pennsylvania focusing on implantable surgical reconstruction products to be used in general surgery applications. With an experienced management team and solid funding, the Company is well positioned to enter the commercial market. Position Overview This position will be the first Clinical Research Ass...
Current Need Clinical Content Analyst - Healthcare IT/Claims Performance Products Position Description The Clinical Content Analyst develops, maintains and supports clinical content for McKesson’s Claims Performance Product Line in a fast paced environment with contractually driven quarterly deliverables. The Claims Performance products are utilized by payer organizations to augment claims managem...
Overview The primary responsibility of the Sr.CPM is to oversee and manage global trials for all clinical phases, in partnership with other functions and the Regional Clinical Trial Managers (RCTMs). The Sr.RCTM is also responsible to provide professional expertise and leadership through leading global departmental tasks, taking initiatives in improving GCO processes and providing mentoring, train...
Overview Initiate and maintain the Clinical QA program in support of Teva's Branded Pharmaceutical Products R&D business Responsibilities Develop and Manage all therapeutic area quality audit programs with the oversight by the Director/Sr. Director Adviser to Clinical trial R&D teams (clin ops, data management, PV, statistics) routine advising independently, advising on major compliance issues wit...
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...
Clinical Dictionary Analyst – The Global Dictionary Analyst is responsible for facilitating Dictionary management processes, including main dictionaries used in clinical data analysis. The Sr. Analyst oversees coding practices, consistency and accuracy across projects, program include: • Ensure timely delivery of appropriate and consistent coding of all clinical study AE and Medication data to fac...
Relevante's client in Reading, PA is actively looking for Project Manager on full-time direct hire basis. Ideal candidate will have experience with clinical application implementation experience in Healthcare Industry. Responsibilities: Under the general direction of the PMO Program Manager/Director, the Project Manager is responsible for the overall planning, management and completion of IT proje...
MedOptions is the leading provider of behavioral health services to residents of nursing homes and assisted living facilities. We service over 600 facilities and 65,000 patients in seven states throughout New England and the Mid-Atlantic states. We expect to add 21,000 more patients in 2014 so we are seeking clinicians who want to provide high quality care and make a difference in the lives of the...
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...
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...
Orthodontic Assistant Join our team for an exciting career in the field of orthodontics to help us create beautiful smiles everyday. We are a well-known and respected orthodontic practice. As a local leader in the industry, we provide a fun working environment for a dedicated professional who enjoys interacting with the public. We offer a competitive benefits package including: PTO (vacation, sick...
Auxilium Pharmaceuticals, Inc is seeking an ETL Developer for its Chesterbrook facility. The ETL Lead/Developer is required to manage all phases of ETL development on assigned projects including creating and reviewing technical documentation, allocating ETL development work, conducting design reviews, coordinating packaging and release deployments and testing of solutions with high volume of proje...
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...
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Healthcare Career Tools
Clinical Coordinator-Clinical Trials
$30,000.00 - $105,000.00
Typical Salary for Clinical Coordinator-Clinical Trials in Pottstown
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
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.
Prepares reports by documenting site observations; maintaining documentation regarding all aspects of the study; developing research reporting protocols and case report forms; coordinating the ongoing monitoring and evaluation documentation of the clinical trial's progress; compiling final study reports.
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