Associate Project Manager, Clinical - 12 Month FTC at United Biosource Corporation
Switzerland, , Switzerland -
Full Time


Start Date

Immediate

Expiry Date

08 Jul, 25

Salary

0.0

Posted On

08 Apr, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Ms Project, Case Report Forms, Management Skills, Communication Skills

Industry

Other Industry

Description

As a pharmaceutical support industry leader, UBC is devoted to empowering health solutions for a better tomorrow. We take pride in improving patient outcomes and advancing healthcare. At UBC, we provide services to enhance the entire drug development process and commercialization lifecycle - From clinical trial support to real-world evidence generation.
We have a great opportunity to join 0ur US team as an Associate Project Manager! Grow your career while making a meaningful impact on the world around you. With a culture built on Collaboration, Conscientiousness, Curiosity, Compassion, and Consultation, we foster an inclusive workplace that fosters creativity.
UBC are looking for a Sr PA or APM for a 12 Month Fixed Term contract position within our fully embedded FSP Model.
Brief Description:

Working independently and reliably showing a high level of ownership, also analytically minded with a strong focus on detail and committed to quality deliverables the Associate Project Manager (APM):

  • Provides operational and technical support to Project Manager (PM), Project Director (PD) and team members of assigned projects during any and all phases of the project.
  • Prioritizes workload/ schedule to meet project needs
  • Supports the PM/PD in facilitating project planning and decision making processes
  • Serves as Lead PM for single/partial scope projects as determined by PD/Department Head
  • Assist PM/PD or independently manage projects per the scopes of work and contracted budgets

DESIRED SKILLS AND QUALIFICATIONS:

  • Excellent interpersonal, verbal and written communication skills
  • Excellent organisational and time management skills
  • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload
  • Analytical mind with high attention to detail
  • Ability to work well and lead a team, as well as working independently
  • Ability to successfully work in a (‘virtual’) team environment
  • Excellent work commitment and client-focused attitude
  • Client focused approach to work
  • Shows commitment to and performs consistently high quality work
  • Proficient in use of web-based IT systems (e.g. CTMS or electronic Case Report Forms) and Microsoft (MS) Excel, MS PowerPoint, MS Project and MS Word
  • Strong working knowledge of medical/scientific terminology and knowledge of ICH-GCP guidelines
  • Knowledge of CRO/Pharmaceutical functional departments and responsibilities
  • Good quantitative skills and working understanding of project budgets
  • Proficient in local language (oral and written) and profound working knowledge of the English language (oral and written)
  • Willingness to travel

EDUCATION/EXPERIENCE:

  • Minimum a Bachelor’s degree or equivalent in a science related field, with an advanced degree desirable, or sufficient, relevant job experience, or another relevant education
  • Ideally 3+ years of Healthcare/ Contract Research Organization (CRO)/Pharmaceutical research/Project Management experience
  • Demonstrated research experience to include at least 3 years as a study coordinator / Project Associate / Clinical Research Associate (CRA) / Lead CRA
Responsibilities
  • Provide internal support to PM / PD as a project resource supporting internal systems and systems set-up but also executing day-to-day data analysis of the operational study status reporting activities
  • Support/Preparation/finalization of project documents and status reports
  • Support/Preparation/finalization of all project plans
  • Support/Preparation of project Microsoft Project (MSP) timelines
  • Support/Prepares draft/final weekly/monthly project reports
  • Support PM/PD in implementing, reviewing, updating project specific metrics, tracking, and reports
  • Support/Compile draft/final study manuals and all study-related materials
  • Arrange project related training and trainings overview and records
  • Assist PM/PD with review of essential project documents
  • Assists in maintenance, quality control, distribution, and archiving of project documents and reports
  • Delegated oversight/Responsible for project TMF preparation, maintenance, and archiving
  • Responsible for preparation, set-up, review of Management Systems, including CTMS, eTMF, web portals, project-specific logs
  • Support PM / PD in set-up of a study specific site/vendor payment procedure
  • Assist PM/PD in ensuring project budgets are tracked against contract milestones
  • Assist Filing, tracking, and logging all project invoicing (sponsor, sites, vendors)
  • Organizes and schedules project team and client meetings
  • Prepares and distributes draft meeting agendas and minutes for project team review
  • Support PM/PD to manage 3rd party vendors (answers queries, provide study updates, etc.)
  • Support PM / PD in appropriate selection of 3rd party vendors and manage procurement process
  • Facilitates communication among team members
  • Communicate with the client on specific items as directed by the PM/PD
  • Lead internal project meetings as directed by PM/PD or dictated by project scope
  • Perform project management related quality checks in co-operation with PM/PD
  • Attend project specific training as required
  • Support PD/PM in preparation for all project audits
  • Complete routine administrative tasks in a timely manner (e.g. timesheets, expenses)
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