Clinical Research Project Manager/Planner (468549) Job in Hamilton, Township Of, New Jersey US

Clinical Research Project Manager/Planner (468549)

Every day, Kelly Scientific Resources (KSR) connects clinical research professionals with opportunities to advance their careers. We currently have an exciting contract opportunity for a Clinical Project Manager (CPM) for our client in Hamilton, NJ. This position will require travel to Jersey City 2 to 4 times per month. As a Clinical Project Manager, you will be responsible for 8 to 12 studies at any given time depending upon the proportion in start up, maintenance and close out. This will include the following responsibilities: Confirm enrollment numbers on the CSSR on a weekly basis Prepare a task list of items due within the week for Team Meeting Agenda, per request of study team Work with functional leads to prepare and plan for critical milestones Provide different timeline scenarios to help team?s prepare for impending milestones Provide Key Milestone dates (or updates) for the Team Meeting Agenda Dependent upon posting frequency, reconcile ROW timelines to Study Timeline Update, review and submit the initial Master User Lists (MULs) to Informatics for upload into MUSE If requested, update Visio slides for Critical Path tasks (weekly while in SSU) Initial entry of a study into CTMS, initial entry of study milestone, update milestones (as needed) and enter actual milestones as achieved For each project assignment, you will meet in house with the other members of the clinical team for various discussions, including Initial and EDC Timeline Review Meetings, as needed. This will be most important in preparation of Critical Milestones, such as: Providing CTMS reports to Director of Clinical Planning on Weekly basis Adding Enrollment graphs to Clinical Planning Folder Working with clinical team to prepare materials and attending monthly Operational Review Committee meetings Anticipating and identifying risks; communicating as appropriate and escalating, as necessary On a weekly basis, the CPM will be required to enter updates in the Pre CSSR (shared drive/Clinical Planning), review the CSSR provided by Project Management Administration, and communication with the study Project Manager, to clarify any updates. You will also provide updates timelines approximately q2 weeks during SSU and FPFV. The CPM will be expected to prepare materials for and participate in various meetings, including Clinical Development Team Meetings, weekly Critical Path Reviews, bi weekly Clinical Planner and Pre CSSR sessions, and monthly PM meetings. You may also attend Team Meetings with CRO and other ad hoc meetings, as requested. SKILLS In order to be successful within this role, qualified candidates must possess strong skills in project management software, such as MS Project, and be able to manage program level timelines. Excellent oral and written communication skills is a imperative as is the ability to work cross functionally across various teams within the CRO and sponsor organizations. EDUCATION/EXPERIENCE Qualified candidates should have a Bachelors degree or licensed certified health care training and at least 4 years of experience working within Clinical Development. Must be able to demonstrate evidence of successfully managing and leading both teams and individuals. A solid understanding of how to craft and manage a project budget is a necessity. A valid passport may be required. If you meet the qualifications and requirements for this position, please Apply Now. Qualified candidates will be contacted. Kelly Scientific Resources has grown into a $270 million global business as the scientific business unit of Kelly Services. Our recruiting consultants place clinical, regulatory and medical affairs, data management and biostatistics professionals to the pharmaceutical, biotechnology, medical device, CRO and university research communities. We invite you to bookmark our Web site and encourage you to review it regularly for new opportunities worldwide: www.kellyscientific.com . Kelly Services is an Equal Opportunity Employer.