Note: The job is a remote job and is open to candidates in USA. UBC is a pharmaceutical support industry leader providing services across the drug development and commercialization lifecycle, including clinical trial support and real-world evidence generation. The Project Manager, SERRM role leads risk management projects, epidemiologic studies, and registries; prepares risk management documents; manages timelines, budgets, deliverables, and client communication; and supports business development activities.
Responsibilities
- Lead and manage the operations of risk management projects, epidemiologic studies and/or registries. Participate as needed in other epidemiology, registries and/or risk management-related projects
- Contribute to preparation, design and writing of Risk Evaluation Mitigation Strategies (REMS), Knowledge, Attitudes and Behaviour (KAB) protocols and surveys, reports, abstracts, and other risk management-related documents in collaboration with physicians and epidemiologists in the department
- Participate in internal and client project teams and meetings
- Observational Program Protocol development
- Coordinate project-related activities, with direct responsibility for ongoing tracking, management of projects and timelines and follow-up of tasks and deliverables
- Coordinate project-related activities with the client and serve as point of contact
- Provide input to Contracts Management group to revise scope of work as needed for projects and budget revisions as required
- Where appropriate, communicate delivery or completion of project deliverables/milestones to Finance to track invoicing and follow-up
- Develop project timelines, schedule project meetings, and develop meeting minutes
- As necessary, working after business hours and on weekends may be required to ensure critical deadlines are achieved (e.g., FDA submissions)
- Support development of proposals – both description of services and budget
- Attend client meetings as needed including bid defense meetings as well as relevant industry meetings
- Present at industry meetings when appropriate
Skills
- Bachelor's degree in life sciences, healthcare, and/or public health or equivalent
- Experience in protocol writing, study design and operations is helpful, as is familiarity with clinical trials, drug development and medical and scientific terminology
- Strong written and verbal communication/ interpersonal skills
- Ability to work independently, yet function well in a small team environment
- Ability to prioritize and work on multiple projects simultaneously
- Knowledge of project management techniques and tools
- Professional, organized, detailed-oriented with a high degree of accuracy, self-motivated and quality driven
- Enjoys fast-paced environment, challenge of learning about different health-related and research areas
- Strong computer skills (word processing, including proficiency with tables and figures)
Benefits
- Remote opportunities
- Growth opportunities for promotion
- 401K with company match
- Tuition reimbursement
- Flexible work environment
- Discretionary Time Off
- Paid Holidays
- Employee assistance programs
- Medical, Dental, and vision coverage
- HSA/FSA
- Telemedicine (Virtual doctor appointments)
- Wellness program
- Adoption assistance
- Short term disability
- Long term disability
- Life insurance
- Discount programs
Company Overview
Company H1B Sponsorship