[Remote] Project Manager - SERRM

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