better Job at PharmaNet Inc

PharmaNet Resource Solutions is the new global alternative for flexible staffing with experienced clinical development professionals. We are currently looking for a contract Technical Assistant (Clinical Research) located in Blue Bell, PA. In this contract position you will: - Provide clerical and administrative support to project teams - Set-up and maintain project files - Set-up and maintain investigator files - Fax, photocopy, and distribute study-related documents - Contact

PharmaNet Resource Solutions is the new global alternative for flexible staffing with experienced clinical development professionals. We are currently looking for a contract Endpoint Management Associate located in Blue Bell, PA. In this contract position you will: - Receive and review Investigator Record of Potential Endpoint or Event forms from Investigator sites - Follow-up with Investigator sites to obtain additional supporting documentation for potential endpoints or events - Review medical

PharmaNet Resource Solutions is the new global alternative for flexible staffing with experienced clinical development professionals. We currently have an exciting opportunity for a Contract Clinical Data Analyst in Cary, NC. - Perform data review and query generation - Define edit checks to be programmed for the study/project - Review programmed edit checks - Track study progress and issue periodic status reports - Update the database to correct errors - Code

- Function as SAS Programmer in our Data Management department - Perform the duties of a Clinical Data Management System (CDMS) support specialist to ensure minimal downtime and quick problem resolution - Troubleshoot CDMS errors - Instruct other Data Management staff in the proper use of CDMS - Report suspected CDMS problems to the vendor's user support group - Implement or ensure the implementation of any necessary fixes to CDMS - Report suspected Oracle problems to PharmaNet

- Act as the Lead Data Analyst for assigned data management project(s) - Coordinate the work of Data Management staff assigned to the project - Train assigned employees on project-related data management procedures and guidelines - Create the data management plan for the study/project - Develop and design Case Report Forms (CRFs) or review sponsor-generated CRFs - Review database structures created by Database Programmers - Define edit checks to be programmed for the study/project - Perform data

PharmaNet Resource Solutions is the new global alternative for flexible staffing with experienced clinical development professionals. We currently have an exciting opportunity for a Contract Clinical Data Analyst in Cary, NC. - Perform data review and query generation - Define edit checks to be programmed for the study/project - Review programmed edit checks - Track study progress and issue periodic status reports - Update the database to correct errors - Code

PharmaNet Resource Solutions is the new global alternative for flexible staffing with experienced clinical development professionals. We are currently looking for a contract Clinical Trial Master File Coordinator located in Princeton, NJ. In this contract position you will be responsible for: - Scanning and electronically publishing regulatory documents - Assisting in the compilation of regulatory submissions, e.g. INDs/CTAs and NDAs/MAAs - Archiving regulatory documents (in both paper and electronic

PharmaNet Resource Solutions is the new global alternative for flexible staffing with experienced clinical development professionals. We are currently looking for a contract Safety Associate located in Princeton, NJ or Blue Bell, PA. In this contract position you will: Process SAE reports Enter Data into ARISg. Job Requirements: Kidney/Renal Disease experience a plus ARISg experience a plus Bachelor s Degree, preferably in a life science or nursing; or RN diploma; in lieu of degree a total of

PharmaNet Resource Solutions is the new global alternative for flexible staffing with experienced clinical development professionals. We currently have exciting opportunities for Contract Regional CRAs. Therapeutic Areas: Pain Management, Vaccine, Immunology, Dermatology, Oncology, Cardiovascular, Ophthalmology Length: 1 year with possible extension Location: Home-based near HUB Airport (i.e. Los Angeles, Chicago, Atlanta, Dallas, Philadelphia, etc). Job Requirements: - Minimum 2 years field monitoring

Serve as System Administrator and Database Administrator for the Learning Management System (LMS) to effect minimal downtime and ensure accuracy of data Design and develop technology-based employee-oriented training materials and programs using a variety of multimedia programs, with particular emphasize on computer and web-based technologies Prepare and conduct appropriate validation/UAT testing for Training Services projects Develop and maintain departmental reports for Training Services Research and

- Serve as the core project team member to coordinate and manage all statistical project activities - Provide statistical liaison with client - Provide statistical input for protocol and CRF development - Prepare statistical analysis plans - Review computer-generated tables to verify accuracy - Prepare key portions of the integrated clinical/statistical report, ISS and ISE, including sections related to data handling and statistical methodology, patient accountability, baseline compatibility, and efficacy

- Perform the duties of a Clinical Data Management System (CDMS) support specialist to ensure minimal downtime and quick problem resolution - Troubleshoot CDMS errors - Instruct other Data Management staff in the proper use of CDMS - Report suspected CDMS problems to the vendor's user support group - Implement or ensure the implementation of any necessary fixes to CDMS - Report suspected Oracle problems to PharmaNet Oracle Database Administrator - May perform some or all of the

- Manage Interactive Voice Response System (IVRS) projects and procedures - Serve as primary contact for assigned IVRS projects - Provide project training to IVRS staff - Define IVRS project specifications with project team and client - Represent and/or promote IVRS functionality during proposal development or bid defense meetings - Present IVRS capabilities at investigator meetings or to potential clients - Monitor IVRS project budgets and timelines - Propose improvements to IVRS functionality and processes