Clinical Data Management Jobs in Pennsylvania
194 Pennsylvania Clinical Data Management jobs found on Monster.Jobs 1 to 20 of 194
Overview Ensures data management activities for clinical trials within assigned research program(s) are completed in a timely and accurate manner Initiates proposal requests to service providers; review vendor proposals and finalize SoW; oversee DM service provider timelines, deliverables, quality and budgets Oversees service providers to perform core data management functions including CRF review...
We are looking for an experienced Senior Data Manager who will ensure on-time compliant execution of all data management activities in support of clinical trials. The scope of responsibilities will include: Work collaboratively with cross-functional teams to develop timelines and define deliverables in support of clinical trials Participation in bid defense meetings Review study specifications and...
My name is Paige, and I represent The Fountain Group. We are a national staffing firm and are currently seeking a candidate for a Sr. Clinical Data Manager position for a prominent client of ours. This position is located in Philadelphia, PA. Details for the positions are as follows: The Senior Clinical Data Manager has extensive industry experience (including EDC) and is responsible for the day t...
Clinical Data Lead This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. As a Clinical Data Lead The lead data management point of contact for day to day activity on a study with key responsibilities for study set-up and close-out tasks as wel...
-Provide support to all clinical research projects with respect to all aspects of administration, coordination, and follow through of deliverables throughout the lifecycle of the project. Provide training and support to other project staff as required. Undertake the development, implementation, and maintenance of projects assigned by the project manager. A. Essential Functions: • Develop a working...
POSITION SUMMARY: This Senior Clinical Operations Specialist is responsible for managing the oversight and implementation of biomarker strategic objectives as directed by the Heme DAS Biomarker Lead. Responsibilities include budget and contract management, sample quality, timeliness and biomarker administrative needs (budget, presentations and study documents). This role is responsible for all bud...
Johnson & Johnson companies are equal opportunity employers. Clinical Product Safety & Performance (1 of 3)-7298130917 Description DePuy Synthes Companies of Johnson & Johnson is seeking a Clinician, Product Safety and Performance (1 of 3) in West Chester, PA. DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the...
Review and modify submission-ready clinical documents by demonstrating high attention to detail, in order to guarantee quality of the final document. Responsibilities cover the following 3 specific areas of Document Quality Review: clinical data checking/consistency checking, clinical editing, and Special assignments/writing projects. Responsibilities: · Independently performs Document Quality Rev...
5yrs+ Managing at a CRO company must be hands on and able to resource Position Summary ESSENTIAL FUNCTIONS: Perform project-related programming Validation and review of other programs Assume responsibilities for data transfers Review Case Report Forms and help in the design of databases Review Report Analysis Plans and provide feedback to the author(s) Mentor less experienced programmers Attend cl...
Overview The incumbent provides regulatory medical writing expertise to the Clinical Pharmacology department in the preparation of clinical research documentation in support of drug development, product registrations, and product marketing. The incumbent oversees/manages/plans the preparation of clinical regulatory documents for specific drug projects, which includes managing medical writing activ...
Our client has a full time opening for a SAS Programmer who will work as a member of Biometrics Department providing statistical support for mainly preclinical and Phase 1 clinical studies. The candidate will closely collaborate with project teams consisting of clinicians, project managers, statisticians, data management and medical writers. Activities include reviewing statistical section of the...
As the only global provider of commercial solutions, Quintiles understands what it takes to deliver nationally and internationally. Our teams help biopharma get their medicines to the people who need them. We help customers gain insight and access to their markets and ultimately demonstrate their product's value to payers, physicians and patients. A significant part of our business is acting as th...
At Care Alternatives we believe that Hospice is for the life we live, and that life should be lived - from its beginning to its end - fully and with great dignity. We follow an individualized holistic approach to Hospice incorporating the Mind, Body, & Soul; done through four different levels of care including Routine, Respite, Inpatient, & Continuous Care. We are in search of a Clinical Services...
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...
Get referred to this job Schedule: Full-time Accenture's Life Sciences practice is dedicated to helping life sciences companies overcome industry challenges, achieve their business objectives and deliver improved health solutions to people around the globe. We serve all the top 10 global pharmaceutical companies, 90 percent of Fortune 500 life sciences companies and more than 125 public health org...
The Judge Group has an opening for Clinical Programmer for a direct client in the Fort Washington, PA area. The full job description is below- if you are interested in applying please send your resume to Will OConnor at the Judge Group ***** . Thanks! 5 or more years experience in pharmaceutical industry (preferred). Develop specifications for analysis datasets, write code for tables,...
ICON Clinical Research Multiple
Home Based Clinical Research Associate Travel up to 80% ( Sites throughout the country) Phase I-IV experience desired Candidate can be based anywhere in the USA Perform assessment site visits to assure study implementation and monitoring activities are conducted according to expectations (as described in the monitoring plan ) The monitor adequately prepares for the Monitoring visit by reviewing si...
ICON Clinical Research Telecommute
· Responsible for obtaining goals of statistical group on clinical research studies. · Develops and implements Statistical Programming Specifications and QC plans with lead Statistician for one or more studies. · Works closely with study team to assure quality data and deliverables are met. · Act as liaison to other groups and teams to relay timelines and goals. · At least 5 years of experience in...
The Judge Group has a immediate opening for a Clinical Programmer for a direct client in Blue Bell, PA. The full job description is below, if you are intrested in applying please send your resume to Will O'Connor at the Judge Group - ***** 5 or more years experience in the US in pharma and CRO (preferred). Develop specifications for analysis datasets, write code for tables, listings a...
BioClinica, Inc., is currently recruiting for a Senior Clinical SAS programmer, specifically with experience in SDTM/CDISC/ADaM programming. This position is located in our Audubon, PA office. The Senior Clinical SAS Programmer is responsible for providing data to clients in a functional format, specifically ensuring the data is compliant with data management standards including SDTM, CDISC and AD...
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I am B.Pharma doing M.Sc(CR)...what kind of jobs i can opt for after done M.Sc in clinical research?
I have heard of CRA,CRC,medical writering,quality assurance etc.....but i want to know how i can enter in clinical research industry at entry level....how i choose the job options as a fresher
Clinical Data Manager or Clinical Project Manager?
I am a Senior Clinical Data Mgr. and I have the opportunity to become a Clinical Proj Mgr. I have an MSc degree. Could someone explain the opportunities that both positions would provide? The Clinical...
For outsourcing Clinical Data Management operations in India which one is better option: CRO or IT?
For outsourcing Clinical Data Management operations in India which one is better option: CRO (Clinical Research Organizations) or IT companies Pharma divisions. In last years some big IT giants have g...
Healthcare Career Tools
Clinical Data Specialist
$31,200.00 - $92,597.00
Typical Salary for Clinical Data Specialist in Pennsylvania
Source: Monster.com Careerbenchmarking Tool
Education / Training
Some College Coursework Completed
Source: Monster.com Careerbenchmarking Tool
Clinical Data Specialist
Maintains data and data quality by helping in the development and maintenance of protocol-specific clinical data management plans.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Attention to Detail
Clinical Lab Testing
Enhances clinical data department and organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.
Develops project-specific data management plans that address areas such as data coding, reporting, or transfer, database locks, and work flow processes.
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