| Job opportunity _ RIM Project Manager _ 100% Remote _ Long Term Contract at Remote, Remote, USA |
| Email: [email protected] |
|
Hi , Greetings from SourceMantra, Please have a look at the below opportunity and reply to me if you are interested. Job: RIM Project Manager Location : 100% Remote Duration: Long Term Contract Need 10+ Years of Experience & Passport Number is must for Submission. Job Description: Key Skill: RIM Suite The Role, We are looking for an experienced consultant with deep expertise in navigating customers through complex software implementation. Veevas Vault RIM suite is the industrys only unified software solution that provides fully integrated regulatory information management (RIM) capabilities including data and document management, submission publishing, and archival on a single cloud-based platform. Veeva Systems is looking for consulting leaders with system implementation experience and a passion for helping customers optimize their regulatory data and document management processes. As a key member of our Professional Services team, the Senior Consultant will be responsible for understanding our customers global regulatory needs, translating requirements into solution design, and defining global strategies for deploying our cloud-based solution for managing regulatory information across the enterprise. Opportunities are available within the United States for this role, which is a remote position. If a candidate is near an airport and able to meet travel requirements, there is no work location requirement. Qualified U.S.-based candidates are encouraged to apply. Requirements 8+ years experience working with life sciences or healthcare companies performing system implementation experience either as a consultant, business, or IT representative In-depth knowledge of drug development processes and regulatory submissions; including, Labeling, Submission Publishing, and/or Viewing systems Proven ability to collaborate and communicate excellently with diverse stakeholders and ensure delivery to a high degree of satisfaction Influential; experience leading teams through hard decisions and negotiating compromises Technical abilities and willingness to roll up your sleeves to design and implement a RIM solution Expert on life sciences compliance and computer systems validation requirements Ability to work independently in a dynamic environment Typical travel is 25% but may be up to 50% based on customer requirements Nice to Have Direct experience with systems such as Veeva Vault, PAREXEL/LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, CARA, Salesforce, Workday, Oracle, SAP, Lorenz Docubridge, Extedo eCTD Manager, Master Control, Trackwise, other regulatory information management or submission publishing systems, etc. Consulting experience, working with a major system integrator or software vendor. Regulatory Affairs, Regulatory Operations, or Pharmacovigilance background. Knowledge of Pharmaceutical, Biotechnology, and/or Medical Device and Diagnostics regulatory processes, data, and content PMP certification Execution experience with Agile methodology and/or ACP Certification Life Science, computer science or related degree SaaS/Cloud experience Locality to major life sciences customer hub (NJ; Boston, MA; San Francisco, CA; Philadelphia, PA; Chicago, IL) Thanks & Regards Sharath Reesu | Source Mantra, Inc. Senior Talent Acquisition 295 Durham Ave, Suite # 201, South Plainfield, NJ 07080 Phone : +1 908 373 8651 Ext: 243 | 732 377 8653 (Fax) [email protected] | www.sourcemantra.com -- Keywords: information technology California Illinois Massachusetts New Jersey Pennsylvania Job opportunity _ RIM Project Manager _ 100% Remote _ Long Term Contract [email protected] |
| [email protected] View All |
| 12:57 AM 08-Feb-25 |