FSP - Project Manager II / Sr. Project Manager - Oncology & Ophthalmology

Fortrea; United States; Remote; USD 140,000 - 185,000; Full time

Benefits offered by this job

Medical insurance

401(k)

Paid time off

Career development opportunities

Job summary

Fortrea is seeking a Senior Project Manager in the United States to lead domestic, regional and global clinical projects. You will manage cross-functional teams and ensure delivery on scope, schedule, cost, and quality.

With 2–5+ years of global PM experience in oncology or ophthalmology, you will partner with client teams, drive risk management, and ensure regulatory data quality. Fortrea offers a collaborative environment and career growth with travel up to 30%.

Qualifications

• 7+ years of clinical research experience in pharma/CRO.
• 2+ years in full project management responsibility.
• Knowledge of ICH Guidelines and GCP.
• Experience in Oncology or Ophthalmology.
• Ability to work in a matrix and virtual environment.
• Excellent communication, planning and organizational skills.

Responsibilities

• Oversee domestic, regional and global projects.
• Lead core project teams and ensure cross-functional collaboration.
• Manage scope, schedule, cost, and quality to contract targets.
• Escalate issues to internal and external stakeholders.
• Develop and monitor KPIs and risk management plans.
• Support line management and talent development.

Skills

Project management

Communication

Leadership

Strategic planning

Regulatory knowledge

Financial awareness

Negotiation

Mentoring

Education

Life sciences degree

Related health certification

Tools

Microsoft Word

Microsoft Excel

Microsoft Project

Microsoft PowerPoint

Access

Job description

Our FSP team is seeking Project Managers/Sr. Project Managers t o join our growing team. This role requires 2-5 + years of global project management experience , with experience in Oncology or Ophthalmology. Candidates must be based in the United States.

Job Overview:

At times working under the direction of a Project Director, the Senior Project Manager oversees and manages domestic, regional and/or global projects. Responsibilities typically include developing and managing project teams, communications, risk, scope, schedule, cost, quality, and stakeholders, effectively ensuring that variance from plan is proactively and effectively mitigated and client expectations are met. The Senior Project Manager is expected to have a working knowledge of drug development and clinical trial execution. They also compile and drive documentation for the project, ensuring the accuracy and quality of regulatory data. The Senior Project Manager may also have line management and / or business development responsibilities.

Summary of Responsibilities:

• Operational delivery.
• Accountable for project delivery with regards to agreed time, scope, cost, and quality.
• TEAM COMMUNICATION: Serve as key client contact for assigned projects, establishing working relationships with client project teams which result in client satisfaction, operational excellence and thereby increase potential for repeat business.
• Lead core project team(s) and facilitate team’s ability to lead extended project team(s), ensuring effective cross-functional teamwork among project team members including both internal and external stakeholders. Depending on size and scope of project(s), this job duty may be performed in collaboration with a Project Director.
• Serve as escalation point for project issues to internal and external stakeholders, as appropriate.
• TEAM COMMUNICATION: Proactively identify and resolve conflicts as needed.
• COST: Understand the project delivery strategy, costing assumptions and resulting budget for assigned project(s).
• SCOPE: Deliver project(s) to scope, schedule, and costs, ensuring all remain on track with the contract and with financial performance targets. Initiate and implement appropriate actions to proactively manage the change control process both internally and externally.
• RISK: Proactively lead both quality control and risk assurance activities to ensure project deliverables are met according to regulatory, Fortrea and client requirements.
• QUALITY: Create and manage variance to required project plans. Per SOPs, implement and monitor progress against project plans and revise, as necessary. Ensure that all staff allocated to assigned project(s) adheres to professional standards and SOPs, providing performance feedback to team member’s respective supervisors.
• Aid in development and maintenance of key project performance indicators for client specified metrics, ensuring that the KPIs are within scope of the project contract.
• Define and manage project resource needs and establish succession plans for key resources.
• Business Development.
• In collaboration with relevant departments, prepare and deliver presentations for new business as required.
• Perform other duties as assigned by management.
• Line Management and Talent Development.
• Trains and mentors PM Academy PCs in multiple areas of expertise.
• May be responsible for Line Management and Talent Development.
• Ensures allocated resources are aligned with current and forecasted work in terms of capability, quantity, timing, and efficiency.
• May be responsible for on-boarding, development, and retention of high performing talent; strengthening and deepening talent bench and succession.
• Assesses project management competencies for assigned staff in order to create developmental plans that will increase competencies and close performance gaps.
• Provides line management and technical support to assigned project leaders, including training, development, and performance review of assigned staff.
• All other duties as needed or assigned.

Qualifications (Minimum Required):

• University/college degree (life science preferred) or certification in a related allied health profession (i.e., nursing, medical or laboratory technology) from an appropriately accredited institution.
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience (Minimum Required):

• Minimum of seven (7) years of relevant clinical research experience in a pharmaceutical company/CRO, including at least two (2) years of full project management responsibility.
• Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
• Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access, and Power Point).
• Experience managing projects in a matrix and virtual environment.
• Excellent communication, planning, and organizational skills.
• Demonstrated ability to lead by example and to encourage team members to seek solutions independently.
• Demonstrated ability to handle multiple competing priorities and to utilize resources effectively.
• Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system.
• Financial awareness and ability to actively utilize financial tracking systems.
• Good knowledge of project management processes.
• Ability to work independently and mentor junior project team members.
• Ability to negotiate and liaise with clients in a professional manner.
• Ability to present to staff at all levels.
• Oncology or Ophthalmology experience

Preferred Qualifications Include:

• Master’s or other advanced degree
• PMP certification
• Biotech experience

What do you get?

Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:

• Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
• 401(K)
• Paid time off (PTO) – Flex Plan
• Employee recognition awards
• Multiple ERG’s (employee resource groups)
• Target Pay Range (based on title of PM II or Sr. PM): $140-185K

#LI - Remote

Applications will be accepted on an ongoing basis.

Work Environment:

• Work is performed in an office environment with exposure to electrical office equipment.
• 30% travel

Physical Requirements:

• Ability to sit for extended periods and operate a vehicle safely.
• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
• Regular and consistent attendance.
• Varied hours may be required.

Learn more about our EEO & Accommodations request here.