Hi, Hope you are doing well.
I would like to check your interest & availability for below mention position. If you are interested kindly reply me back with your updated resume, contact details & best time to reach you. Project Manager Location: New London, CT area; Bridgewater, NJ area; Greater Philadelphia, PA area Duration: 9 Month Contract Phone Hire *Job Description:* The Project Manager (PM) will manage the integration plans (e.g., deliverables, risks, issues) for FDA Regulatory, Content Management, Clinical Trials, Safety and Centralized Services IT M&A Integration activities. PM will be deeply involved in improving the quality, predictability and efficiency of the Information Management integration delivery capability. Ensure that the operational issues of the integrations are managed, focusing on the project interface with project leaders, project teams, and integration team. • Oversee IT Mergers & Acquisitions projects/programs execution. • Define and manage plans and timelines • Risk management, including risk assessment for the overall program • Ensure proper execution of the risk plan throughout the projects lifecycle • Perform data mapping from source to target systems • Lead a geographically distributed team • Manage and deploy initiatives by influence *Key Deliverables:* • Integrated project plan for the program • Status reports • Communication decks • Communication Plan • Data migration/transfer plans • Product Template (includes Product and study data) • Cross functional dependency plan • Manage SharePoint meeting space • Create and manage Risk register *Qualifications:* • 5+ years of Program/Project Management experience, or 3-5 years of equivalent leadership experience • 15 years of Integration and Pharmaceutical Business/Industry work experience including an understanding of Clinical, Safety, Regulatory and Content Management systems and processes. • Must possess extensive knowledge and expertise in program/project management, portfolio management, and integrations • Must have experience in migration analysis, and documentation. • Expertise in Microsoft Office Suite including Visio. • Bachelor’s degree or higher desired. *Tools and Technologies:* • Clinical: EDC (Oracle Clinical), Registry (RTII), Analysis and Reporting (CDARS) • Regulatory: Product and Licensing (PEARL), Submissions (eCTD) • Content Management: Document Management (GDMS) • Safety: Pharmacovigilance System (ARGUS) *Waiting for your response…* Best Regards, *Ravi Nigam* 978-558-4666 Ext. 101 r...@teknavigators.com *TekNavigators LLC* 100 Cummings Center, Suite 207 P, Beverly, MA 01915 DISCLAIMER: This message and any attachments are solely for the use of the individual or entity to which it is addressed and may contain information that is privileged or confidential. If you are not the intended recipient, any disclosure, use or distribution of the information contained herein is prohibited. If you have received this communication in error, please notify the sender by reply e-mail and immediately delete this message and any attachments. You may reply and send an email with "Remove" in the subject line in order to discontinue communication. -- You received this message because you are subscribed to the Google Groups "SAP Workflow" group. To unsubscribe from this group and stop receiving emails from it, send an email to sap-workflow+unsubscr...@googlegroups.com. To post to this group, send email to sap-workflow@googlegroups.com. Visit this group at https://groups.google.com/group/sap-workflow. For more options, visit https://groups.google.com/d/optout.
