Clinical Trials Program Manager
Company: Vitalief Inc.
Location: New Brunswick
Posted on: May 7, 2022
Vitalief is a fast growing, "best of breed" Clinical Trial
Solutions Company. We are seeking a problem-solving oriented
Clinical Trials Program Manager to join our exceptional team, that
has a passion for building new relationships within existing client
accounts, gaining credibility by supporting our clients in planning
and execution of successful clinical trials; and manage Vitalief's
consulting resources to maximize employee retention. Every trial is
different and requires a solution that will optimize outcomes. Our
approach explores innovative ways of delivering services in a
distributed model that can support both decentralized and
If you are interested in being part of a culture that includes the
ability to have a voice challenging the status quo with novel
thinking, flexible work environment, transparent and open
communications, career pathing, and a variable incentive / reward
system, then we want to speak with you!
NOTE: This is a hybrid position (mostly remote / partial work at
client site); must be commutable to the New Brunswick, NJ area.
Establish and maintain a positive partnership with our clients
Clinical Trials Office (CTO), work cross functionally internally
and externally, communicating with all stakeholders, managing
client expectations and ensuring successful clinical trials and
overall client satisfaction.
Provide full life cycle management for our clinical trials
services, that includes workforce planning, resource allocation;
workflow process improvement, as well as the evolution of
additional value add service offerings in partnership with
Responsible for all phases of life cycle management of the service
and to ensure continuous improvement efforts are dedicated to
delivering high performing, reliable, and consistent operations and
developing cohesive culture-based teams while optimizing costs and
Standardize work intake processes, prioritizing work, and all
aspects of workforce planning including ensuring direct reports are
adequately trained, aligning resources with appropriate assignments
and managing team performance.
Provide structure, guidance and support for budget planning and
staffing for delivery of service.
Consistently communicate with each team member to ensure they are
achieving business objectives; and they are in alignment with their
professional development objectives.
Effectively positioning yourself and Vitalief as a highly valued,
trusted delivery partner with client executives and management.
10 or more years of overall experience with a primary focus in the
clinical operations in the pharmaceutical industry, CRO or
Must have 4 years of clinical trials domain management level
experience as a Senior Clinical Research Associate (CRA), Lead CRA,
CRA Manager, Project Manager, Operations Manager, and/or Program
Excellent understanding of the concept and application of Good
Ability to operate effectively within a smaller, high-growth
solutions consultancy; prioritize tasks and manage multiple
priorities, meet deadlines, and be flexible to changing priorities
Excellent leadership and management skills, with a collaborative
approach to driving performance and success in a distributed work
environment; strong employee retention skills.
Direct experience managing Clinical Research Associates is
Sound project planning/management, workforce planning and resource
Proven track record of building long standing, valuable client
relationships, ensuring successful project delivery and customer
Highly driven, results oriented, competitive, positive person who
thrives in a small, team oriented, fast paced, entrepreneurial
Bachelor's degree is required.
Keywords: Vitalief Inc., New Brunswick , Clinical Trials Program Manager, Executive , New Brunswick, New Jersey
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