Project Manager, Study Operations, Cronos in United States at Jobgether

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Project Manager, Study Operations, Cronos based in the United States.

This role sits at the center of clinical study delivery, leading the execution of clinical projects that bring new therapies to patients faster and more efficiently. You will oversee study operations from planning through completion, ensuring alignment with contractual requirements, quality standards, and operational timelines. Acting as a key point of coordination across cross-functional teams, you will drive collaboration, manage risks, and ensure consistent delivery against study milestones. The position combines strategic oversight with hands-on project leadership in a fast-paced, global clinical research environment. You will also engage directly with clients and internal stakeholders, supporting communication, performance tracking, and issue resolution. This is a high-impact role where strong leadership, organization, and clinical expertise directly influence study success and patient outcomes.

Lead and manage clinical study operations from initiation through closeout, ensuring delivery excellence across scope, timeline, quality, and budget expectations.

• Develop and maintain integrated study management plans in collaboration with cross-functional project teams.
• Oversee execution of clinical studies in accordance with contracts, SOPs, regulatory requirements, and internal quality standards.
• Serve as the central coordination point for study teams, aligning objectives, tracking performance, and ensuring milestone achievement.
• Manage project risks, issues, and contingencies, implementing mitigation and corrective action plans as needed.
• Monitor study progress and proactively report updates to internal stakeholders and clients.
• Support bid defense activities and contribute to proposals for smaller or regional studies when required.
• Lead cross-functional collaboration across clinical operations, vendors, and internal functional groups.
• Ensure financial oversight of assigned studies, including scope management and change control processes.
• Act as primary or backup client contact for assigned studies, maintaining strong customer relationships.
• Mentor junior team members and support capability development within project teams.
• Identify process improvements and contribute to best practice adoption across study operations.

Candidates should bring strong clinical project management experience, cross-functional leadership skills, and the ability to deliver complex studies in a global environment.

• Bachelor’s degree in Life Sciences or related field required.
• 7+ years of clinical research experience, including approximately 5+ years in clinical project management.
• Strong understanding of clinical trial operations and global study execution.
• Proven ability to manage multiple stakeholders and lead cross-functional teams in a matrix environment.
• Experience in client-facing roles, including study oversight and relationship management.
• Strong problem-solving skills with the ability to manage risks, issues, and competing priorities.
• Excellent communication, presentation, and interpersonal skills.
• Ability to interpret complex information and make sound, timely decisions.
• Strong knowledge of clinical trial processes, SOPs, and quality standards.
• Experience managing study budgets, timelines, and change control processes.
• Ability to mentor junior staff and support team development.

• Competitive base salary ranging from $93,100 to $232,800, depending on experience, qualifications, and location.
• Eligibility for performance-based bonuses and incentive plans.
• Comprehensive health coverage including medical, dental, and vision insurance.
• Retirement savings plans and financial wellness programs.
• Paid time off, holidays, and flexible work arrangements (remote eligible).
• Parental leave and family support benefits.
• Training, certification, and professional development opportunities.
• Employee wellness programs and support resources.
• Opportunities to work on global clinical trials with high-impact outcomes.