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