Director, Project Management - Autoimmune

Reposted 3 Days Ago
Be an Early Applicant
Hiring Remotely in Canada
Remote
180K-270K Annually
Expert/Leader
Biotech
The Role
Lead and oversee global clinical program project management teams for autoimmune studies. Provide strategic oversight, resource allocation, risk mitigation, stakeholder escalation, budget and KPI management, talent development, and business development support to ensure delivery of quality, scope, cost, and timeline objectives across clinical study projects.
Summary Generated by Built In

Position Summary: 

Works cross functionally to develop partnership strategies for clinical trials and programs and works closely with our project teams to provide oversight, strategic expertise in the planning, coordination, and delivery of all activities for designated clinical study projects to ensure that project objectives of quality, scope, cost, and time are accomplished. 

Essential functions of the job include but are not limited to:  

  • Direct, manage and ensure collaboration within a team Project Directors and Project Managers in the planning, execution and governance of projects/portfolios on a global platform
  • Provide leadership and oversight on all clinical programs and in some unique cases, manage activities 
  • Interact with study sponsors as primary point of escalation beyond project management
  • Optimize the profitability of the Project Management organization to meet or exceed budget targets
  • Assess and manage resource allocations to ensure that established cost, time, and quality goals are met
  • Select, train, develop and manage the performance of talent in project leadership positions (Project Directors and Project Managers)
  • Provide technical support and guidance (including scope definition, risk identification, escalation and mitigation, resource planning, goals and deliverables) to assigned project managers
  • Identify and escalate impacts to project scope, resources, schedule or budget through standard methods
  • Ensure project leadership personnel work to the highest quality standards and maintain compliance with established SOPs, working guidelines, project plans and all regulatory requirements
  • Participate with Business Development in opportunity development, proposals and budgeting, bid defense preparation and attendance
  • Understand and manage project/program inter-dependencies to achieve program milestones/deliverables 
  • Conduct evaluations and implement required changes for all projects (including mid-project recovery of at risk projects, re-scoping, postponement, or cancellation)
  • Measure and report KPIs and lead continuous improvement
  • Recognize, exemplify and adhere to Precision’s values that center on our commitment to quality, our people, clients and performance
  • Manage workload of supervised staff with continued assessment and adjustment as needed
  • Provide on-going feedback, development and coaching of Project Directors and Project Managers including annual performance reviews

Qualifications: 

Minimum Required: 

  • Bachelor’s degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred.
  • A minimum 10 years of experience in clinical research, including extensive project management and line management experience or proven competencies for this position
  • Working knowledge of GCP/ICH guidelines and the clinical development process

Other Required: 

  • Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project 
  • Excellent communication and interpersonal skills to effectively interface with others in a team setting 
  • Excellent organizational skills, attention to detail, and a customer service demeanor 
  • Ability to travel domestically and internationally including overnight stays 

Preferred: 

  • Advanced degree 
  • Experience in managing complex and global trials 

Competencies:  

  • Working knowledge of project management techniques and tools 
  • Direct work experience in a global, cross-functional project management environment 
  • Proven experience in people management 
  • Proven experience in strategic planning, risk management and change management 
  • Ability to work closely with business unit leadership to understand customer's needs 
  • Strong analytical skills and business acumen 
  • Executive presence with ability to confidently deliver complex presentations to senior management 
  • High level of integrity and must inspire and demand the highest standards from a professional and ethical perspective. 
  • Demonstrated leadership track record and effective interpersonal skills 
  • Ability to lead and inspire excellence within a team 
  • Ability to create an environment where employees have a sense of ownership that will lead to increases in productivity and efficiency 
  • Results oriented, accountable, motivated and flexible 
  • Excellent time management, negotiation, critical thinking, decision making, analytical and interpersonal skills 
  • Excellent presentation, verbal and written communications skills 
  • Proficient in project management software  
  • In depth proven experience in pharmaceutical and/or device research required 
  • Excellent Planning and organizing 
  • Excellent at influencing and leading 
  • Proven experience in delegating while fostering cohesive team dynamics  
  • Demonstrated successful independent negotiation and conflict management strategies
  • Preferred experience with Autoimmune and Oncology 

Salary Range: 180,200 - 270,400/yr CAD (Salary based on experience) 

#LI-KH1 #LI-Remote





Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [email protected] so we can investigate and take appropriate action.

Skills Required

  • Bachelor's degree or equivalent in science or health-related field
  • Advanced degree
  • Minimum 10 years of experience in clinical research including project management and line management
  • Working knowledge of GCP/ICH guidelines and the clinical development process
  • Experience with Microsoft Outlook, Word, Excel and PowerPoint
  • Experience with Microsoft Project
  • Proficient in project management software
  • Excellent communication and interpersonal skills
  • Excellent organizational skills, attention to detail, and customer service demeanor
  • Ability to travel domestically and internationally including overnight stays
  • Experience managing complex and global trials
  • Proven experience in people management
  • In-depth proven experience in pharmaceutical and/or device research
  • Preferred experience with Autoimmune and Oncology
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The Company
HQ: Bethesda, MD
1,114 Employees

What We Do

Precision is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. This maximizes our clients’ insight into patient biology, delivering more predictable trial outcomes and accelerating clinical development. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe.

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