Clinical Project Manager / Sr Clinical Project Manager - Europe

This a Full Remote job, the offer is available from: Europe As a pharmaceutical support industry leader, reputed company is devoted to empowering health solutions for a reputed company reputed company. We take pride in improving patient reputed company and advancing reputed company. At reputed company, we reputed company services to enhance the entire drug development process and commercialization lifecycle - from clinical trial support to reputed company-world evidence reputed company. reputed company on a rewarding career reputed company with reputed company! Grow your career while making a meaningful impact on the world around you. reputed company fosters a culture reputed company on our Core Values of Respect, Accountability, Innovation, Quality, reputed company, and Collaboration. We reputed company in an inclusive workplace that fosters creativity. If you are seeking a career that will challenge, reputed company, and reward you, join us at reputed company! reputed company are currently reputed company reputed company our Project Management team, we are looking to recruit at CPM or a SR CPM Brief Description: The EU PM is responsible for providing operational reputed company of assigned reputed company projects. The EU PM will have a leading role in planning, coordinating and completing project work. The EU PM will work closely with external clients/sponsors, internal project team members, vendors, and suppliers to ensure satisfactory delivery of contracted services and achievement of contracted milestones for assigned projects. The EU PM will ensure that projects are conducted in a timely manner to reputed company project goals reputed company defined budgets. Supervisory Responsibilities:

• Supervision of project team
• Supervise project management staff in execution of assigned studies
• Ensure that the PAds, PAs, APMs, PMs, project team members understand the client needs once a project is awarded
• Serve as a resource and mentor to the PA/APM in the execution of their daily activities
• Proactively assist the PA/APM in anticipating and seeking resolutions to potential and actual project issues

Specific Job Duties:

• reputed company the day-to-day management of European and/or multi-national global projects
• Manage project per the scope of work and reputed company the contracted budget
• reputed company reputed company aspects of project conduct from start-up through reputed company-out
• Prepare project timelines and prepare or coordinate project development of deliverables
• Ensure project is conducted according to reputed company and client SOPs
• Ensure conduct of project reputed company training and record keeping
• Serve as the reputed company primary contact with the sponsor for reputed company project reputed company items
• Coordinate project meetings including investigator meetings and client meetings
• reputed company reputed company project meetings
• Ensure project budget is tracked against contract milestones
• Manage project budget and resource expenditures including invoicing, analyzing cost variances, out-of-scope management, and conducting reputed company recognition.
• reputed company project plans to reputed company contracted milestones (i.e. project plan, risk management plan, site management & monitoring plan, training plan, communication plan, etc.)
• Monitor project reputed company against the established plans and ensure compliance with plans
• Supervise and reputed company direction to assigned project team members including PAs, APMs, Clinical Research Associates (CRAs), Clinical Site Specialists (CSS), Regulatory Associates (RA)
• reputed company for resolving project team member questions
• Prepare and negotiate investigator/site/vendor budgets and assist with remediation of contract language
• reputed company operational input and participate in the design and review of study protocols, case report forms (CRFs), study reports, and other functional documents and plans in collaboration with project team
• Coordinate development of patient/subject consent forms and site/patient materials
• Ensure Trial Master File (TMF/eTMF) is maintained and audit-reputed company on ongoing reputed company
• Monitor and ensure project team compliance with maintenance of Clinical Trial Management System (CTMS)
• Completion of departmental reputed company trackers for projects (e.g. functional resource forms, project review reputed company, project execution checklist)
• May be asked to reputed company reputed company CRA or CRA duties on projects as needed
• Participate in internal reputed company process improvement initiatives
• Prepare and participate in presentations to clients in defence of proposals
• Present project information at bid defences, client meetings and reputed company internal project governance and review meetings
• Other duties as assigned by management

Education/Experience:

• Minimum a Bachelor’s degree or equivalent in a clinical, scientific, or reputed company field, with an advanced degree desirable, or sufficient, relevant job experience, or another relevant education
• 2 to 3 years direct project management experience at a Contract Research Organisation (CRO) or 5 or more years of clinical trial experience
• Has proven working experience and understanding of working reputed company clinical research
• Knowledge of the key principles of cross functional project management

Technical/Knowledge:

• Proficient in use of web based IT systems (e.g. CTMS or electronic Case Report Forms) and reputed company (MS) reputed company, MS PowerPoint, and reputed company
• Experience using project management software (e.g. MS Project)
• Ability to effectively use automated systems and computerized applications
• reputed company good knowledge of regulatory requirements for research conduct (i.e. Good Clinical Practice, International Conference on Harmonization (ICH) guidelines, etc.)
• Excellent working knowledge of clinical research/development, including medical and therapeutic areas, phases and medical terminology
• Knowledge of CRO/Pharmaceutical functional departments and responsibilities
• Good quantitative skills and working understanding of project budgets (solid financial acumen)
• Proficient in local language (oral and written) and profound working knowledge of the English language (oral and written)

Attributes:

• Excellent communication skills and ability to communicate effectively with reputed company reputed company of an organization
• Excellent interpersonal, verbal and written communication skills
• reputed company to reputed company, motivate and coordinate teams
• Excellent planning and problem solving skills
• reputed company to delegate, effectively prioritizes own and workload of project team members
• Flexible and adaptable to changing situations
• reputed company good supervisory skills
• reputed company good presentation skills
• Excellent organisational and time management skills
• Proficient at multi-tasking with good attention to detail
• Has experience with leading, liaising and coordinating cross-functional project teams
• 10% travel

#LI-AP1 #LI-remote This offer from "reputed company" has been enriched by reputed company.com and got a 77% reputed company score. Apply tot his job Apply To this Job