Senior Project Manager - Oncology

Precision For Medicine; Peapack-Gladstone (NJ); On-site; USD 147,300 - 220,900; Full time

Benefits offered by this job

Discretionary annual bonus

Health insurance

Retirement savings benefits

Life insurance

Disability benefits

Parental leave

Paid time off

Job summary

Precision Medicine Group seeks a Senior Project Manager to lead clinical study activities, ensuring quality, scope, cost, and time objectives are met. You will act as the main client contact and oversee vendors to maintain timelines and budget.

Responsibilities include managing budgets, coordinating cross-functional teams, ensuring inspection readiness, and delivering regular status updates to clients and senior management.

Qualifications

• Bachelor’s degree or equivalent in science/health field; advanced degree preferred.
• 7+ years clinical research experience and 4+ years direct PM experience.
• Experience managing complex/global trials.
• Willingness to travel domestically and internationally.

Responsibilities

• Serve as primary client contact and escalation point.
• Coordinate external vendors to timeline and budget.
• Manage study budget; identify out-of-scope activities early.
• Ensure quality management and inspection readiness (eTMF).
• Lead meetings, report KPIs, and propose solutions.
• Provide training and development feedback to team.

Skills

Client communication

Budget management

Risk management

Leadership

Cross-functional teamwork

Negotiation

Strategic planning

Education

Bachelor’s degree in science or health-related field

Advanced degree preferred

Tools

Microsoft Office

Microsoft Project

eTMF

EDC

CTMS

Job description

The Senior Project Manager plans, directs, coordinates, and delivers 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:

• Serve as primary point-of-contact and primary escalation point to the client
• Coordinate and oversee all functional services including external vendors to the established timeline and budget
• Manage the study budget, ensuring project remains within scope and that any out of scope activities are identified early and handled as appropriate. Independently drive the CO to completion and execution with support as needed.
• Maintain integrated collaboration with clinical operations in the delivery and participate in clinical activities as appropriate. For projects of very limited scope (i.e., number of sites), Sr. PM may assume all clinical activities
• Manage the financial health of assigned studies, including oversight of the project profitability, billable project hours, and compliance with on time, accurate billing and forecasting to support business objectives.
• Develop robust and comprehensive project plans, including timelines and proactive risk management and mitigation, to guide all parameters of trial execution with consistency and quality
• Ensure quality management for assigned projects, including eTMF inspection readiness, implementation of quality notification incident forms and/or corrective and preventive action plans to address any quality findings.
• Maintain integrated collaboration with all functional operations in the delivery of the program and review as necessary of other study documentation
• Establish tracking metrics to monitor trial and team progress towards project goals
• Prepare project status updates and report on progress to clients and senior management, including reporting on key performance indicators, offering solutions and opportunities as they arise
• Lead both internal and client meetings and set expectations for the project team
• Communicate effectively with client and Precision management to relay protocol/study issues including any deviations and implement necessary actions in response to those issues
• Ability to conduct formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients including bid defenses with proficiency
• Ensure study specific training is implemented in collaboration with functional areas and ensure study specific training compliance for the duration of the project
• Support business development and marketing activities as appropriate, including travel to bid defense meetings as required
• Perform other duties as assigned by management
• Remain compliant with organizational training, time‑reporting and any other administrative duties as required
• Provide ongoing feedback for functional team members including annual performance reviews

Qualifications

Minimum Required

• North America: Bachelor’s degree or equivalent combination of education/experience in science or health‑related field. Advanced degree preferred
• EU: Degree or equivalent combination of education/experience in science or health‑related field. Advanced degree preferred
• Minimum of 7 years of clinical research experience or proven competencies for this position and a minimum of 4 years of direct project management experience
• Experience in managing complex and global trials
• Ability to travel domestically and internationally including overnight stays

Other Required

• Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project, eTMF, EDC and CTMS
• Proven communication and interpersonal skills to effectively interface with others in a team setting
• Proven organizational skills, attention to detail, and a customer service demeanor

Competencies

• Demonstrates knowledge of ICH‑GCP, relevant Precision SOPs, and the ability to implement such items
• Direct work experience in a global, cross‑functional project management environment
• Good understanding of cross‑functional management
• Good understanding of project planning, risk management and change management with an awareness of appropriate escalation
• Proven experience in strategic planning, risk management and change management
• High level of integrity and must inspire and demand the highest standards from a professional and ethical perspective
• Ability to lead and inspire excellence within a study team
• Ability to create an environment where study team members have a sense of ownership that will lead to increases in productivity and efficiency
• Results oriented, accountable, motivated and flexible
• Proven time management, negotiation, critical thinking, decision making, analytical and interpersonal skills
• Proven presentation, verbal and written communications skills
• Good understanding of project management software
• In‑depth proven experience in pharmaceutical and/or device research required
• Radiopharmaceutical trial experience strongly preferred
• Preferred: experience with oncology & cell and/or gene therapy

Reasonable estimate of the current range: $147,300 USD – $220,900 USD. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

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.