better Biotech Pharma Job in Pennsylvania

Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators Negotiate study budgets with investigators Obtain, review, and process regulatory and administrative documents from investigator sites Review and develop protocols Review and develop

Our client has an immediate opening for a "Contractor" Biostatistician who will provide all aspects of design and statistical analyses and reporting on clinical development projects. Insure timely completion of statistical analyses and reports. Responsibilities: Participates in the design, analysis and reporting of research studies (Phase II Phase IV); provides consultation on experimental design and statistical research approaches, requirements and scientific standards. Develops statistical

Clinical Trials Research Associate / Research Associate I (Part-time) Job Type: Part-Time Location: Philadelphia, PA Job Description: Clinical Trials Research Associate (ACRIM) 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

Biostatistician II - Clinical Trials Job Type: Full-Time Location: PHILADELPHIA, PA Job Description: The American College of Radiology seeks a Biostatistician to collaborate in the design, monitoring, analysis, and reporting of all phases of cancer treatment clinical trials involving radiation therapy. The ACR serves as headquarters for the Radiation Therapy Oncology Group (www.RTOG.org). The RTOG is a national cancer study research group funded by the NCI, with almost 40 years of experience in running clinical

Smith Hanley has an outstanding new opportunity for a Clinical Research Coordinator for our client in Chadd s Ford, PA. The successful candidate will assist several different Clinical Project Managers with the following: - Budgeting tasks - Populating a study - Assisting with study questionnaires - Assisting in completing CRF's - Documenting adverse events - Following up on SOP's (assisting to make certain people are trained on new SOP's.) - The chosen candidate will be working on clinicaltrials.gov

Job Summary For assigned studies, provides oversight and support to clinical operations team in planning, conduct, and closeout of assigned clinical studies assuring consistency across regions and compliance with GCP/ICH and study objectives. Provides sponsor oversight of clinical monitoring activities including site initiation and management, document management, study training, safety reporting, and oversight of regional leads and field CRAs including management of trip report review and issue resolution

DUTIES: -Identifies, evaluates and selects study centers -Obtain, review for appropriateness and process regulatory and administrative documents from study sites -Maintain clinical files -Track progress and status of contractual agreements (non-disclosure agreements, clinical trial agreements, contracts with vendors) -Manages central IRB, where applicable -Process/track safety information (IND Safety Reports/SAE Reports) to ensure regulatory compliance and real-time reconciliation of the clinical trial and

Clinical Community Pharmacist Department: WellSpan Infusion Services Schedule: Full time (80hrs/2wks) Shift: Hours: provide pt centered care for home infusion pts Job Details: General Summary: Under general supervision, provides pharmaceuticals and drug information as needed for adequate patient care according to professional standards and practices. Duties and Responsibilities: The following are essential job accountabilities: 1 Compounds pharmaceutical preparations and/or labels and packages medications

Biostatistician Mar 5 2008 Kennett Square Pennsylvania Return to Search Results Send job to...

Director Biostatistics May 30 2008 Philadelphia area Pennsylvania Return to Search Results Send job to...

health care programs in Western and Central Pennsylvania Western Tennessee Ohio Delaware South Carolina and...to practice Pharmacy in the State of Pennsylvania B S...

Clinical Data Manager Req. Code : CDM/PA Division/Department : UBC - Late Stage Location : 1. BLUE BELL PA US 19422 2. KANSAS CITY MO US 64111 Travel Required : None Job Type : Full Time Career Level : Manager (Manager/Supervisor of Staff) Education : Bachelor's Degree Category : Biotechnology and Pharmaceutical Job Description : Manages clinical data to meet project needs. · Responsible for all support operation specialists’ duties should the need arise · Responsible for delivering quality

Biostatisticians Req. Code : NWTN_Stats Division/Department : UBC - Biotechnology Solutions Location : Newtown PA US Travel Required : None Job Type : Full Time Career Level : Experienced (Non-Manager) Education : Bachelor's Degree Category : Biotechnology and Pharmaceutical Job Description : Employees Create the Evidence that Matters As demand for the rapid delivery of new pharmaceuticals, biotechnology and medical devices to identify, treat and prevent disease is on the rise, never has the need for conclusive

Senior Clinical Project Manager Req. Code : 301 Division/Department : UBC - Late Stage Location : BLUE BELL PA US 19422 Travel Required : None Job Type : Full Time Career Level : Manager (Manager/Supervisor of Staff) Education : Bachelor's Degree Category : Biotechnology and Pharmaceutical Job Description : Lead UBC project teams to deliver project milestones. Supervision of project team Oversee all aspects of trial conduct from Study Start-up through Close-Out Manager project per the scope of work and

Senior Clinical Programmer/Analyst I Req. Code : 75 Division/Department : UBC - Biotechnology Solutions Location : NEWTOWN PA US 18940 Travel Required : None Job Type : Full Time Career Level : Experienced (Non-Manager) Education : Bachelor's Degree Category : Biotechnology and Pharmaceutical Job Description : Essential Duties and Responsibilities: Write, modify, and maintain programs which produce data sets, tables, and listings for assigned projects Write, modify, and maintain programs that perform complex

Clinical Project Manager Fort Washington Pennsylvania Return to Search Results Send job to...

Position Description: The Lead Clinical Data Analyst functions as a pivotal member of a multi-disciplinary clinical reporting team whose expertise spans the domains of clinical data systems and reporting, clinical practice, and research processes. The Lead Clinical Data Analyst will generally extract and transform data from a variety of clinical and supporting non-clinical data sources to enable research and operational initiatives across a rapidly evolving academic research enterprise. This position will

Associate Director / Director, Clinical Research, Oncology CLI001841 Job Description Submit Description Merck & Co. Inc., established in 1891, is a global research-driven pharmaceutical company dedicated to putting patients first. Join us and experience our culture first-hand one of strong ethics & integrity, diversified experiences and a resounding passion for improving human health. As part of our global team, you ll have the opportunity to collaborate with talented and dedicated colleagues while

Job Title: Clinical Research Coordinator Specialty: N/A Department: Office of Research Licensure: N/A Description: Looking for a fabulous new career opportunity? No previous experience needed. Clinical Research Coordinators work within Academic Affairs in the newly formed Office of Research at The Reading Hospital and Medical Center. Research Coordinators are responsible for recruiting patients for clinical trials, regulatory document processing, and interaction with trial sponsors. Coordinators maintain

Profile Locations USA Pennsylvania Philadelphia Organization USA02 US Clinical Development Svcs...

Profile Locations USA Pennsylvania Pittsburgh Organization USA02 US Clinical Development Svcs...

Profile Locations USA Pennsylvania Philadelphia Organization USA02 US Clinical Development Svcs...

Profile Locations USA Pennsylvania Organization USA02 US Clinical Development Svcs...

Profile Locations USA Pennsylvania Philadelphia Organization USA02 US Clinical Development Svcs...

Clinical Pharmacist GLC Associates has an exciting new opportunity for a DUR Clinical Pharmacist. This position is a Monday - Friday Day shift position. NO Weekends ! ! Excellent Benefits and a great work environment. The Clinical Pharmacist will be responsible for : - Conducting extensive reviews and evaluations of DUR Programs - Performing letter and phone interventions - Performing quality control checks on intervention letters - Documenting communication

A Clinical Data Manager is currently being sought for a contract position in Exton, PA. The Clinical Data Manager is responsible for the quality and timeliness of all data management activities for a study by preparing validation plans and chairing validation meetings. The position will prepare material for presenting at investigator meetings and will identify errors and inconsistencies in CRF data and ensure their resolution. The CDM will be responsible for study startup documents, data cleaning, query tracking

At Wyeth, we have a vision of leading the way to a healthier world. We've committed ourselves to achieving this vision by making quality, integrity and excellence the hallmarks of our business. A Fortune 500 company and global leader in pharmaceuticals, consumer healthcare, and animal healthcare products, we know that our employees are who keep us on the cutting edge of innovative discoveries and superior customer service. To sustain and enhance our leadership position in the pharmaceutical industry, we continue

Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites Review draft protocols for completeness and feasibility Develop Case Report Forms for clinical trials Present (e.g

Research Neuroscience will be based in Collegeville Pennsylvania and report to the Assistant Vice President...

Reporting to the Senior Director, Biometrics, the Clinical Data Management Specialist will review clinical trial data to identify erroneous, missing, incomplete or implausible data. This will be accomplished by running ancillary programs in Oracle Clinical database software and also by carrying out query production, resolution and tracking to resolve problematic data identified during manual review or electronic edit checks. When you work for Smith Hanley Consulting Group, you are partnering with a leader

You would need to be located in or willing to relocate to the Blue Bell Philadelphia Pennsylvania area...

The Clinical Project Manager will engage in large multi-product, multi-facility clinical systems implementation projects for our client company. Position requires frequent interaction with customers, multiple teams, outside vendors and suppliers, and multiple cross-functional Services teams. Seasoned project management and executive client communication skills are required.. Job Requirements: PMP certified Proficiency in clinical workflow, ideally across departments and systems Proven leadership

Job Description: At Wyeth, we have a vision of leading the way to a healthier world. We've committed ourselves to achieving this vision by making quality, integrity and excellence the hallmarks of our business. A Fortune 500 company and global leader in pharmaceuticals, consumer healthcare, and animal healthcare products, we know that our employees are who keep us on the cutting edge of innovative discoveries and superior customer service. To sustain and enhance our leadership position in the pharmaceutical

Qualifications Pennsylvania Pharmacy license Doctor of Pharmacy degree PGY...

Entry-level clinical research assistant. Recruits participants and coordinates scheduling and follow-up. Conducts data collection with research participants. Maintains a status report to be reviewed by the Principal Investigator and/or Research Coordinator. Assists in data collection, storage and data entry. Participates in grant related meetings with Principal Investigator or Research Coordinator and research team when appropriate to gain a better understanding of protocol issues and project developments

Responsibilities: A Clinical Data Manager is currently being sought for a contract position in Exton, PA. The Clinical Data Manager is responsible for the quality and timeliness of all data management activities for a study by preparing validation plans and chairing validation meetings. The position will prepare material for presenting at investigator meetings and will identify errors and inconsistencies in CRF data and ensure their resolution. The CDM will be responsible for study startup documents, data cleaning

ClinForce is currently seeking a Lead Clinical Data Manager for Conshohocken, PA. Successful candidate will be responsible for the following: - Data Management leadership on large and/or multiple projects with responsibility for the development of the project Data Management Plan; data management systems set-up; and data accession, data entry and data review specifications and processes; oversight of data management activities for the delivery of clinical data according to client quality and integrity

Job Classification: Contract Description: DUTIES: -Identifies, evaluates and selects study centers -Obtain, review for appropriateness and process regulatory and administrative documents from study sites -Maintain clinical files -Track progress and status of contractual agreements (non-disclosure agreements, clinical trial agreements, contracts with vendors) -Manages central IRB, where applicable -Process/track safety information (IND Safety Reports/SAE Reports) to ensure regulatory compliance and real-time

ClinForce is currently seeking a Lead Clinical Data Manager for Conshohocken, PA. Successful candidate will be responsible for the following: - Data Management leadership on large and/or multiple projects with responsibility for the development of the project Data Management Plan; data management systems set-up; and data accession, data entry and data review specifications and processes; oversight of data management activities for the delivery of clinical data according to client quality and integrity specifications

A Clinical Data Manager is currently being sought for a contract position in Exton, PA. The Clinical Data Manager is responsible for the quality and timeliness of all data management activities for a study by preparing validation plans and chairing validation meetings. The position will prepare material for presenting at investigator meetings and will identify errors and inconsistencies in CRF data and ensure their resolution. The CDM will be responsible for study startup documents, data cleaning, query tracking

ISS Solutions, a strategic affiliate of the Geisinger Health System and a specialized Clinical Engineering provider centered in the mid Atlantic region, is currently seeking a District Operations Manager for the Clinical Engineering Maintenance Program. This position will be based in Wilkes Barre, PA and will supervise and manage service technicians to ensure timely completion of all technical operations within the North East area(s). Some of the many responsibilities will be to insure overall user satisfaction

ISS Solutions, a strategic affiliate of the Geisinger Health System and a specialized Clinical Engineering provider centered in the mid Atlantic region, is currently seeking a District Operations Manager for the Clinical Engineering Maintenance Program. This position will be based in Wilkes Barre, PA and will supervise and manage service technicians to ensure timely completion of all technical operations within the North East area(s). Some of the many responsibilities will be to insure overall user satisfaction

Job Requirements Qualifications Pennsylvania Licensed Pharmacist At least one year hospital experience CareerBuilder Related Terms PharmD Hospital Pharmacist Clinical...

Assume primary responsibility to collect details of adverse events received by phone or mail for ethicals and biologics and perform initial assessment according to local procedures and in accordance with company global drug safety procedures. Create initial reports by directly entering information into Drug Safety databases, amend reports and enter follow-up information as acquired, and prepare report for FDA submission. Maintain continuous knowledge expertise in local and global requirements for safety reporting

We have a regular full-time (80 hours bi-weekly) position available in the Radiation Oncology department in Thomas Jefferson University Hospital. The Clinical Research Coordinator III responsibilities may include developing grant opportunities, processing and tracking all IRB and sponsor-required documents, mentoring investigators in the IRB process and keeping track of certifications for all personnel.. Job Requirements: - B.A or B.S. degree preferred or commensurate oncology research experience. - Certified

Job Classification: Contract Description: Job Summary For assigned studies, provides oversight and support to clinical operations team in planning, conduct, and closeout of assigned clinical studies assuring consistency across regions and compliance with GCP/ICH and study objectives. Provides sponsor oversight of clinical monitoring activities including site initiation and management, document management, study training, safety reporting, and oversight of regional leads and field CRAs including management

PRA International is a world leader in providing clinical research services to the pharmaceutical and biopharmaceutical industries. We serve some of the best-known companies in the world and work on many of the most advanced experimental drugs, Biologics and medical devices in development today. We currently have an excellent opportunities for a Clinical Project Manager and Clinical Project Directors. These positions can be office based at any of our US locations in NJ, PA, VA, KS, TX, and CA or now can be regionally

PRA is one of the world s leading clinical development organizations with more than 2,700 employees worldwide providing reliable service delivery, program-level therapeutic expertise, easy global access to knowledge and involved senior management to our customers. Over the past 25 years, we have earned the confidence of the pharmaceutical and biotechnical industries through our unique approach we call Project Assurance : our company-wide commitment to consistently achieve our customers requirements everywhere

LOCATION: North America- West Coast, North East, and Midwest SUPERVISOR: Director, Clinical Operations North America SUMMARY: I Pre-Study Period A. Tasks Identify potential investigators for studies to be initiated. Participate in pre-study and study initiation visits. Ensure completeness and compile regulatory documents (e.g. IRB approval, informed consent, lab certification etc.). Coordinate study material

Research Associate to their team in Pittsburgh Pennsylvania...