[Hiring] Senior Clinical Project Manager @Rho Inc

Role Description

We are currently hiring a Sr. Project Manager to join our team! As a Senior Project Manager here at Rho, you’ll have the opportunity to grow your career and provide leadership to cross-functional clinical research projects and team members. You’ll need to provide on-time, on-budget, and high-quality project results as well as:

• Motivating, training, and mentoring team members
• Helping develop new superior customer experiences while maintaining Rho’s core values, including Teamwork, Quality, Great People, among others
• Leading complex projects and developing junior staff

Therapeutic expertise in any of the following is preferred:

• Central Nervous System (movement disorders, psychiatry)
• Pain (post-surgical pain)
• Respiratory
• Food Allergy

This is a remote position within the US with the willingness to travel for sponsor visits, meetings, and trainings, as needed.

Responsibilities

• Lead large, global, and/or complex clinical trial projects, conceptualizing the execution strategy for each component project
• Prepare project management plans and other governance documents
• Recommend and implement operational strategies as well as risk management plans
• Manage assigned project resources, including ensuring that project tasks are correctly assigned to staff and vendors
• Manage project and vendor budgets and scope of work, including recognizing and negotiating changes in scope
• Make tactical recommendations to customers to improve projects and provide strategic and tactical guidance to team members
• Mentor and provide training and orientation for team members
• Manage team dynamics and provide frequent feedback to team members
• Collaborate with customers to provide win/win solutions
• Contribute to business development initiatives, including proposals, responses to RFIs, and bid defense presentations

Qualifications

• BS in life sciences or related field
• Minimum 5 years’ experience managing progressively larger and more complex clinical research projects
• Solid understanding of applicable clinical research and scientific concepts and regulatory requirements (e.g., Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, regulatory agency regulations)
• Ability to interpret study protocols and designs
• Experience in conducting on-site monitoring visits and/or managing activities of a CRA team to achieve project deliverables
• Strong communicator: Demonstrate written, verbal, and presentation skills
• Committed to quality: Attention to detail and understanding of high-quality scientific standards
• High-character: Contribute to a collaborative culture with honesty and integrity
• Critical thinker: Evaluate situations and opportunities objectively and craft novel, practical solutions
• Agile and adaptable: Ability to change quickly and manage risks

Benefits

• Comprehensive benefits package including medical, vision, dental, HSA, FSA, EAP, life & disability insurance, and 401(k)
• Paid time off, holidays, parental leave, and bereavement leave
• Encouragement of work-life balance

Compensation

The range of starting pay for this role is $110,000-$150,000 per year. Actual compensation is influenced by a wide array of factors including role responsibilities, location, candidate skill set, and level of experience.