Vertex Pharmaceuticals
Associate Director - Regulatory Project Management (Contract) 24525
Vertex Pharmaceuticals, Myrtle Point, Oregon, United States, 97458
Employer Industry: Life Sciences Regulatory Affairs
Why consider this job opportunity
Salary up to $100/hr
Opportunity for career advancement and growth within the organization
Remote work opportunity with flexibility in working hours
Engage in critical regulatory submission activities that impact the broader organization
Work in a collaborative environment focused on achieving key project milestones
Benefit from a supportive management structure with potential financial accountabilities
What to Expect (Job Responsibilities)
Oversee complex project and portfolio plans from initiation to closeout
Drive the definition of project milestones, tasks, deliverables, and resource requirements
Lead strategies for risk mitigation and contingency planning within project plans
Manage project status, issues, schedules, and accomplishments, communicating updates to stakeholders
Supervise members of the submission management team and prepare necessary reports for resource discussions
What is Required (Qualifications)
Bachelor’s degree in life sciences or a technology-related field
Typically requires 10+ years of project management experience in regulatory/clinical project management or within a life sciences company
Minimum of 2 years of supervisory/management experience
Expertise in global regulatory filing project management and project management tools
Excellent organization, communication, and stakeholder management skills
How to Stand Out (Preferred Qualifications)
Experience using Veeva Rim for content plan submissions
Comprehensive understanding of global health authority submissions and guidelines
Proven ability to adapt quickly to changing requirements and priorities
Strong attention to detail and ability to persuade management to take action
Experience balancing multiple tasks to meet priorities and timelines
#LifeSciences #RegulatoryAffairs #ProjectManagement #RemoteWork #CareerOpportunity
We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top‑tier employer.
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Why consider this job opportunity
Salary up to $100/hr
Opportunity for career advancement and growth within the organization
Remote work opportunity with flexibility in working hours
Engage in critical regulatory submission activities that impact the broader organization
Work in a collaborative environment focused on achieving key project milestones
Benefit from a supportive management structure with potential financial accountabilities
What to Expect (Job Responsibilities)
Oversee complex project and portfolio plans from initiation to closeout
Drive the definition of project milestones, tasks, deliverables, and resource requirements
Lead strategies for risk mitigation and contingency planning within project plans
Manage project status, issues, schedules, and accomplishments, communicating updates to stakeholders
Supervise members of the submission management team and prepare necessary reports for resource discussions
What is Required (Qualifications)
Bachelor’s degree in life sciences or a technology-related field
Typically requires 10+ years of project management experience in regulatory/clinical project management or within a life sciences company
Minimum of 2 years of supervisory/management experience
Expertise in global regulatory filing project management and project management tools
Excellent organization, communication, and stakeholder management skills
How to Stand Out (Preferred Qualifications)
Experience using Veeva Rim for content plan submissions
Comprehensive understanding of global health authority submissions and guidelines
Proven ability to adapt quickly to changing requirements and priorities
Strong attention to detail and ability to persuade management to take action
Experience balancing multiple tasks to meet priorities and timelines
#LifeSciences #RegulatoryAffairs #ProjectManagement #RemoteWork #CareerOpportunity
We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top‑tier employer.
#J-18808-Ljbffr