Hi,
Please find the requirement below and answer ASAP with updated resume and contact details to *[email protected]* ...Thanks a lot... ------------------------------------------------------------ Resumes with the following information will be given preference. Full Name: Current Location: Relocation: Availability: Work Authorization in US: Contact Number: Email: Rate on C2C: Please ensure all candidates have all skills listed under "Required Skills" in their resume. ---------------------------------------------------------------- *US Citizens or GC Holders only.* Title: Oracle Clinical Study Designer Right to Hire: Yes Contract Duration: 6 months Location: Princeton, New Jersey Minimum Requirements: • Bachelor's Degree in Life Sciences, Pharmacy or Nursing or equivalent experience • Formal or on-the-job training in clinical trial methodology and Good Clinical Practice (GCP) • Minimum of three years expert-level experience with Oracle Clinical, with the most recent being with Oracle Clinical/RDC 4.5.x • Strong experience with Oracle Database administration activities • Extensive CRF design experience, firm understanding of user interface design principles • Team player who can multi-task, work effectively with members of other teams, and communicate productively with clients • Experience in a regulated environment, especially pharmaceutical (21 CFR Part 11), • Good time management and organization skills; the ability to prioritize own work to meet tight deadlines while maintaining the highest standards of work Description: This person will design and create Oracle Clinical studies in conjunction with the Oracle Clinical developers, clinical data coordinators, and study project team leaders. This includes leveraging pre-existing GLib data objects, creation of new objects, creation of validation documents, and delineation of procedure requirements. Responsibilities • Design, create, and validate new studies in Oracle Clinical; this includes data object configuration, Glib maintenance, CRF design, and validation documentation • Integrate protocol and charter requirements with internal business practices to draft Study Data Quality Plans • Manage validation and deployment of new studies • Plan and manage the update and re-validation of amended studies • Delineate requirements and scheduling of data listings and patient data reports • Liaise with Data Management, Clinical Operations, submission team, business development, and medical affairs groups • Document activities and work according to SOPs. Write clearly and accurately • Mentor junior colleagues, engender knowledge transfer * * *Regards, Kumar Reddy,* *Resource Specialist* * OSAIR Technologies LLC 301 N HARRISON STREET SUITE # 386 Princeton,NJ | 08540-3512 Voice : 630-206-9379* *Fax :732-289-6076 [email protected]* *www.osairtech.com* *"We want to be your Trusted, Preferred & long Term Partner"* *Note: If you are not interested in receiving our e-mails then please reply to [email protected]<http://mail.osairtech.com/cgi-bin/compose.exe?id=01991591c8ba56cc62e720994fb077a65d18&new=&xsl=compose.xsl&[email protected]>with a "remove" in the subject line and mention all the e-mail addresses to be removed with any e-mail addresses, which might be diverting the e-mails to you. Apologies for the inconvenience caused.* --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "Oracle-Distribution" group. To post to this group, send email to [email protected] To unsubscribe from this group, send email to [email protected] For more options, visit this group at http://groups.google.com/group/Oracle-Distribution -~----------~----~----~----~------~----~------~--~---
