Senior Project Manager - Oncology

  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 oversees 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 participates 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 preventative 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     Leads 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 implements 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   Provides on-going 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, as well as 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 #LI-KH1 #LI-Remote         Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case.  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. Reasonable estimate of the current range $147,300 — $220,900 USD Any data provided as a part of this application will be stored in accordance with our  Privacy Policy.  For CA applicants, please also refer to our  CA Privacy Notice . 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. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com . Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.

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