Director Project Management
EPM Scientific are looking for a top level candidate to fill a vacancy as a Director, Project Management for an ON SITE Role. As a Director of Project Management, you will play a crucial role in client facing project management. Working closely with cross functional drug development team, you will drive the client based projects forward and ensure project deliverables are completed on time and on... schedule. We are seeking a motivated and skilled individual who is passionate about the future of science.
Job Title: Director, Project Management
Location: Alachua, FL
Role type: Full time (Temp to Perm)
Main Responsibilities:
Lead the US PM group as a role model and mentor
Establish best PM practices and tools that impact the company culture and performance
Create culture of high performing teams with clear accountabilities, robust scientific debate and respectful interactions that foster trust.
Lead site projects including tracking of deliverables, development of timelines, and run effective project meetings
Build relationships in the organization that foster collaboration, teamwork and achieving company objectives
Lead cross-functional programs and project meetings
Build fully integrated timelines capturing all activities and resources needed to deliver individual program and corporate goals
Monitor program progress and identify risks and opportunities to timeline, budget, or scope
Identify clear program objectives, success criteria and recommend risk mitigation actions
Drive program teams towards the delivery of project milestones on time, on budget, and within scope through utilization of project management tools
Work with finance and teams on monthly billables and forecasts
Represent the team at decision meetings, company presentations and interactions with external parties such as Health Authorities or partners.
Requirements:
Advanced science degree preferred
10 years biotechnology or pharma experience, with at least 5 years specifically in program leadership/ management
Experience in leading cross functional teams through early clinical studies (Phase I/II)
Motivated individuals who want to roll up their sleeves and apply drug development knowledge and experience to develop gene-editing therapies
Looking for individuals who embrace taking accountability for team dynamics, planning and deliverables
Benefits:
Annual bonus
401k
Medical, Dental, Vision, Life, Short-Term and Long-Term Disability, AD&D, and additional insurances
20 days PTO
5 days Sick leave
6 weeks Parental Leave
Next Steps:
Please send over any up to date resumes and relevant info!
Kind regards
Apply Now
Job Title: Director, Project Management
Location: Alachua, FL
Role type: Full time (Temp to Perm)
Main Responsibilities:
Lead the US PM group as a role model and mentor
Establish best PM practices and tools that impact the company culture and performance
Create culture of high performing teams with clear accountabilities, robust scientific debate and respectful interactions that foster trust.
Lead site projects including tracking of deliverables, development of timelines, and run effective project meetings
Build relationships in the organization that foster collaboration, teamwork and achieving company objectives
Lead cross-functional programs and project meetings
Build fully integrated timelines capturing all activities and resources needed to deliver individual program and corporate goals
Monitor program progress and identify risks and opportunities to timeline, budget, or scope
Identify clear program objectives, success criteria and recommend risk mitigation actions
Drive program teams towards the delivery of project milestones on time, on budget, and within scope through utilization of project management tools
Work with finance and teams on monthly billables and forecasts
Represent the team at decision meetings, company presentations and interactions with external parties such as Health Authorities or partners.
Requirements:
Advanced science degree preferred
10 years biotechnology or pharma experience, with at least 5 years specifically in program leadership/ management
Experience in leading cross functional teams through early clinical studies (Phase I/II)
Motivated individuals who want to roll up their sleeves and apply drug development knowledge and experience to develop gene-editing therapies
Looking for individuals who embrace taking accountability for team dynamics, planning and deliverables
Benefits:
Annual bonus
401k
Medical, Dental, Vision, Life, Short-Term and Long-Term Disability, AD&D, and additional insurances
20 days PTO
5 days Sick leave
6 weeks Parental Leave
Next Steps:
Please send over any up to date resumes and relevant info!
Kind regards
Apply Now