better Biotech Pharma Job in Pennsylvania

The person in this role be involved in the design of Phase I-IV clinical trials. S/He will develop statistical analysis plans and write statistical methods sections for protocols. S/He will also perform the appropriate sample size estimation and do power calculations to determine specific trial hypotheses. In addition, s/he will work with SAS programmers in creating analysis results for study reports. S/He will interface with data managers to ensure the quality of case report forms and final data. S/He may serve

Title Clinical Research Associate City Philadelphia State Pennsylvania Scheduled Shift Days Employee Type Regular Part...

Title Clinical Research Asst City Philadelphia State Pennsylvania Scheduled Shift Days Employee Type Regular Part...

Our US site is located in Swiftwater Pennsylvania among the scenic Pocono Mountains sanofi pasteur...

BUSY PRACTICE SEEKS EXPERIENCE MEDICAL RESEARCH COORDINATOR TO WORK ALONE IN SATELLITE OFFICE. MUST BE FAMILIAR WITH ALL REGULATORY COMPLIANCES. INVOLVED IN CASE STUDIES. TRAINING IN PITTSBURGH. WILL TRAVEL 4 TIMES A YEAR.. Job Requirements: College Grad with Medical research experience.

Clinical Pharmacist Coordinator Department: Pharmaceuticals Schedule: full-time (1.0 FTE - 80 hours per payperiod) Shift: 1st Hours: Pay Grade: 95 Job Details: Job Summary:This position serves as an expert resource in pharmacotherapy. This position is responsible for developing and maintaining a patient centric clinical pharmacy practice model which includes the training, mentoring and ongoing evaluation of pharmacist clinical activities. This position also optimizes drug therapy both patient specific

Welcome to Genesis HealthCare! We're setting the standard for clinical excellence and responsiveness in meeting the unique needs of every resident and patient in our care. We're focused on becoming the recognized leader in clinical quality and customer satisfaction in every market we serve. Position Description: Genesis HealthCare is one of the nation's largest providers of skilled nursing and rehabilitation therapy. To fulfill our mission of providing high quality healthcare, clinical support is available

Clinical Data Project Manager: The Clinical Data Project Manager will be responsible for all areas of project management related to the implementation of EDC based clinical studies. Such responsibilities include requirements gathering from the customer to planning, scheduling internal resources for eCRF programming, data management, training materials as well as being the primary project interface for our Pharmaceutical customers for selected projects. Company Description: Numoda is a life

At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philosophies. Using these tools, Kforce is able to better plan and anticipate work loads and thus minimize the peaks of work that can swamp you

At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philosophies. Using these tools, Kforce is able to better plan and anticipate work loads and thus minimize the peaks of work that can swamp you

08 PM Functional area Scientific Location Collegeville Pennsylvania Required degrees Doctorate Professional Experience required Not...

46 PM Functional area Clinical Location Pittsburgh Pennsylvania Required degrees Bachelor s Level Degree Experience...

Our client, a large hospital network, is looking for a Clinical Research Coordinator in Philadelphia, PA. This position works with study protocols, screening and enrolling patients and laboratory activities including working directly with patients. On a day-to-day basis, this person will be responsible for new study activities including: -Obtaining detailed knowledge of all components of study protocol through independent analysis and review of study and related literature, prior to study start date. -Assuring

At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philosophies. Using these tools, Kforce is able to better plan and anticipate work loads and thus minimize the peaks of work that can swamp you

The incumbent is responsible for hands-on management of Phase I clinical trial data in both a paper system and an electronic data system. Examples of tasks include data integrity review, discrepancy generation and resolution. Must effectively liaise with all functional areas that interact with clinical data. Must be able to work independently or with minimal supervision.. Job Requirements: Leadership skills with ability to create and work in high performance teams and/or matrix organization. Must be able to

Clinical Research Asst I City Philadelphia State Pennsylvania Scheduled Shift Days Employee Type Regular Full...s Hospital of Philadelphia and University of Pennsylvania research community...

management situated in the Lehigh Valley of Pennsylvania develops manufactures and markets in vitro diagnostic...

is preferred Country USA State Province Region Pennsylvania Site Location Field Research Employer of Choice...

The incumbent is responsible for hands-on management of Phase I clinical trial data in both a paper system and an electronic data system. Examples of tasks include data integrity review, discrepancy generation and resolution. Must effectively liaise with all functional areas that interact with clinical data. Must be able to work independently or with minimal supervision. Leadership skills with ability to create and work in high performance teams and/or matrix organization. Must be able to collaborate to resolve

Title Clinical Operations Manager NOVOCART Division State Pennsylvania City Center Valley Job Description Aesculap is...Our U S corporate office is located in Center Valley Pennsylvania...

We are seeking a Clinical Research Coordinator III position in the Department of Radiation Oncology at Thomas Jefferson University Hospital.. Job Requirements: The incumbent would ideally have the following qualifications: BA/BS or higher CCRP, CCRC, or CTR Knowledge of oncology clinical research (radiation oncology preferred) Experience working directly with patients Ability to multi-task in a demanding, intense work environment Experience with regulatory and protocol development Excellent

We are seeking a Clinical Research Coordinator III position in the Department of Radiation Oncology at Thomas Jefferson University Hospital. The incumbent would ideally have the following qualifications: BA/BS or higher CCRP, CCRC, or CTR Knowledge of oncology clinical research (radiation oncology preferred) Experience working directly with patients Ability to multi-task in a demanding, intense work environment Experience with regulatory and protocol development Excellent computer skills

ClinForce is currently seeking a Clinical Research Coordinator - CRC for Philadelphia, PA. Successful candidate will be responsible for the following: - Work directly at patient/subject interface at investigational sites to deliver high quality patient data in accordance with regulations and as required by the study protocol. - Participate in the recruitment and screening of research participants. - Design and maintain organizational tools to conduct the research study accurately in compliance

active pharmacy license in good standing in Pennsylvania AZ or TN...

Joul Clinical Staffing Solutions is the premier provider of clinical research professionals to the pharmaceutical and biotechnology industries. We offer dynamic and challenging job opportunities within organizations recognized as leaders within their industries. We are currently recruiting for a Clinical Research Associate to work on a project at one of our clients near Plymouth Meeting, PA. The position involves the following type of work: Monitoring sites for two clinical trials, including site initiations

At Covance, your imagination, your dedication, and your drive to find solutions to challenging projects begin on your very first day. Covance is one of the world s largest and most respected contract research organizations. Our clients are a Who s Who of the pharmaceutical and biotechnology industry. If you re looking for a diverse and stimulating work environment, you'll find it at Covance. Currently we have an exciting opportunity for a Senior Manager, Clinical Data Management. As a Senior Manager, Clinical

Clinical Research Associate I Requisition Number: 24211 Union: NON-UNION Department: Dermatology Administration Schedule: Full-Time (72hrs per pay period) Shift: Day Shift Hours: 8am - 5pm Job Details: JOB SUMMARY: Responsible for assisting with the implementation of clinical research protocols under Physician Investigator and/or Clinical Research Specialists and coordinators. Participate in a variety of activities involved in the analysis, collection, compilation, and documentation of clinical research data

Clinical Trials Data Specialist Requisition Number: 24199 Union: NON-UNION Department: Hematology Oncology Clinical Trials Schedule: Full-Time (80hrs per pay period) Shift: Day Shift Hours: 8:00 am - 5:00 pm Job Details: JOB SUMMARY: Responsible for research protocol data management processes, including data acquisition, entry and reporting. JOB REQUIREMENTS: Associate's degree in a technical or administrative program, specialized training of over 18 months and up to 3 years or equivalent knowledge with

The Biostatistician will be responsible for the following duties, among others: Provides input on design of studies and reviews protocols Computes sample sizes in conjunction with clinical staff as required for clinical studies Writes detailed analysis plans and analyzes clinical data, as directed by immediate supervisor Designs summary tables, reports, and graphs for presentation of results Writes statistical analysis descriptions for protocols and final reports, as directed by immediate supervisor

The Biostatistician will be responsible for the following duties, among others: Provides input on design of studies and reviews protocols Computes sample sizes in conjunction with clinical staff as required for clinical studies Writes detailed analysis plans and analyzes clinical data, as directed by immediate supervisor Designs summary tables, reports, and graphs for presentation of results Writes statistical analysis descriptions for protocols and final reports, as directed by immediate supervisor

than 650 000 people in south central Pennsylvania and northern Maryland...

Every day, Kelly Scientific Resources (KSR) connects scientific professionals with opportunities to advance their careers. KSR is the first and largest scientific staffing company in the world, and we currently have an exciting Medical Pharmacovigilance Associate position available northwest of Philadelphia, PA. A Medical Pharmacovigilance Scientist applies their skills, knowledge, and experience to contribute to the overall safety surveillance of marketed and investigational products. The principle responsibilities

Our U S corporate office is located in Center Valley Pennsylvania...Our U S corporate office is located in Center Valley Pennsylvania...

UPMC Cancer Centers works in tandem with the University of Pittsburgh Cancer Institute, which comprises the academic and research activities for cancer at the University of Pittsburgh and UPMC, to offer patients the latest advances in cancer prevention, detection, diagnosis and treatment. We are currently recruiting full-time clinical research coordinators (CRCs) for a variety of specialties at the UPMC Hillman Cancer Center in the Shadyside area of Pittsburgh. The specialties include: melanoma, sarcoma

Kforce is seeking an experienced Early Clinical Development Specialist in North Wales, PA. Responsibilities: - Assist with the design and conduct of clinical studies with emphasis on the protocol/TA specific aspects of the protocol - Perform medical monitoring of study data - Ensure appropriate input from clinical research physician and senior clinical research specialist staff - Support Clinical Sciences and other functional areas in the development of clinical study deliverables - Pursue relevant

Clinical Trials Research Associate/Research Associate I (ACR-Image Metrix P-349) Job Type: Full-Time Location: Philadelphia, PA Job Description: Research Associate- Clinical Trials ACR Image Metrix (www.acr-imagemetrix.net) is a subsidiary of the American College of Radiology (www.ACR.org), the premier healthcare society committed to ensuring that imaging is safe, effective, and accessible to all patients. The ACR's clinical research division in Philadelphia has been the leading research organization in radiology

Clinical Project Manager Job Code: 23046 Facility: UHS of Delaware Inc - Corporate Office Location: KING OF PRUSSIA, PA US Travel Involved: None Job Type: Full Time Job Level: Minimum Education Required: Bachelor's Degree Skills: Category: Information Technology FTE: 1.0 Position Summary: Manages the implementation of UHS applications. Manages all aspects of projects assigned from preparing project schedules and estimates through final implementation. Oversees modifications to existing applications that

For almost 100 years, Pocono Medical Center has been serving our community, enriching the lives of not only our area residents, but also the many people who have built careers with us. Over the years we have steadily grown from a small general hospital to a 247-bed regional medical center. Thoracic Nurse Navigator/Clinical Research Associate Cancer Center Utilize your 5+ yrs of nursing experience to manage patient flow within the clinic; scheduling diagnostic exams and organizing separate treatment

Please note: All applicants must apply via PittSource, the University of Pittsburgh's on-line employment system, as we no longer accept paper or e-mailed resumes/applications. To apply for this position click the following link: www.pittsource.com/applicants/Central?quickFind=63405 This position is for a registered nurse or other healthcare related degree (i., e., respiratory therapy) with experience in critical care medicine. Experience in clinical trial research preferred

Yoh Clinical is seeking a top-notch Senior Clinical Project Manager - IVD for a contract role with our customer in the Philadelphia, PA area. Duties: - This position is located in Raleigh/Durham, NC. - Our customer is an established clinical diagnostics company with a number of products in clinical trials and on the market. They are seeking a contract Senior Clinical Project Manager to supplement their team. - The incumbent will be responsible for the overall management of clinical trials

Title Clinical Research Assistant City Philadelphia State Pennsylvania Scheduled Shift Days Employee Type Regular Full...

At the University of Pennsylvania Health System our pharmacists do more than dispense medications...A current Pharmacist license to practice in Pennsylvania is essential...Working within the University of Pennsylvania Health System you will enjoy the camaraderie...

Otsuka Pharmaceutical Development and Commercialization, Inc. (OPDC) is involved in conducting all phases of clinical research and development of innovative healthcare products to address unmet medical needs. OPDC is well established in the scientific community as a globally focused organization that plays a leadership role in the research and development of Otsuka's ethical healthcare products. The Company is dedicated to the improvement of the quality of human life and health of patients around the world

Summary The Clinical Supply Project Manager (CSPM) organizes all activities involved with the management of clinical supplies. This includes but is not limited to the following services: procurement, distribution, formulation/development, manufacturing, packaging and analytical services. The CSPM serves as the primary business partner contact. It is the responsibility of the CSPM to define the scope and timing of the requested services. The CSPM coordinates all internal and external communication relative

active pharmacy license in good standing in Pennsylvania AZ or TN...

REGIONAL CLINICAL RESEARCH ASSOCIATE (CRA) Integrium is an established contract research organization providing a comprehensive range of clinical trial services to the biopharmaceutical and medical device industries. At Integrium, we combine cutting-edge science and practical operational management to bring innovative ideas to all aspects of the workplace. Integrium is currently seeking regional CRAs to join our growing Field Operations team. We are specifically looking for someone based in the area

equivalent 2 years effective experience An active Pennsylvania RN license PREFERRED QUALIFICATIONS Experience in a...

31 AM Functional area Clinical Location Collegeville Pennsylvania Required degrees Not Indicated Experience required Not...

Reference # : 09-03217 Title : Clinical Data Analyst Location : King of Prussia, PA Experience Level : Start Date : Tue, Oct 20, 2009 Description Providing technical support and assistance to clinical study teams, enabling them to deliver high quality clinical trial data. This role is centred around the development, deployment and maintenance of the eCRF data capture package but is also heavily involved with the extraction, manipulation and reporting of eCRF and non-eCRF data. A working knowledge of GCP and

The Clinical Trials Center of the VA Pittsburgh Healthcare System is recruiting for a clinical research coordinator to staff a multifaceted clinical research program. The incumbent will coordinate and implement procedures according to study protocol including screening, administering informed consent, conducting protocol related visits consisting of but not limited to collection, processing and shipment of blood specimens as well as collecting data from patient medical records, interviews, questionnaires