Senior Project Manager – Oncology

🔥 24 minutes ago

🇺🇸 United States – Remote

💵 $147.3k - $220.9k / year

⏰ Full Time

🟠 Senior

👷‍♀️ Project Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 11%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

• Just posted.
• Jobs at this company usually fill in 34 days.

Apply Now

Find Similar Remote Jobs

Precision Medicine Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Plan, direct, coordinate, and deliver activities for designated clinical study projects • Serve as the primary client point of contact and escalation point • Coordinate functional services and external vendors according to timelines and budgets • Manage study budgets, scope, out-of-scope activities, and change orders • Collaborate with clinical operations and participate in clinical activities as appropriate • Manage study financial health, profitability, billable hours, billing, and forecasting • Develop project plans, timelines, risk management, and mitigation strategies • Ensure project quality, eTMF inspection readiness, quality notifications, and corrective/preventive action plans • Collaborate with functional operations and review study documentation • Establish tracking metrics for trial and team progress • Prepare status updates and report KPIs and progress to clients and senior management • Lead internal and client meetings and set project team expectations • Communicate study issues and deviations and implement necessary actions • Conduct formal presentations, including bid defenses • Implement and monitor study-specific training compliance • Support business development and marketing activities, including travel to bid defense meetings • Provide ongoing feedback and annual performance reviews for functional team members • Complete assigned duties, organizational training, time reporting, and administrative requirements

🎯 Requirements

• 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 • Minimum of 4 years of direct project management experience • Experience managing complex and global trials • Ability to travel domestically and internationally, including overnight stays • Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project, eTMF, EDC and CTMS • Proven communication and interpersonal skills • Proven organizational skills, attention to detail, and customer service demeanor • Knowledge of ICH-GCP and relevant Precision SOPs • Direct work experience in a global, cross-functional project management environment • Understanding of cross-functional management • Understanding and proven experience in project planning, risk management and change management • Time management, negotiation, critical thinking, decision-making, analytical and interpersonal skills • Presentation, verbal and written communication skills • Understanding of project management software • In-depth proven experience in pharmaceutical and/or device research • Experience with oncology and cell and/or gene therapy preferred • Must be legally authorized to work in the country of employment without employer sponsorship

🏖️ Benefits

• Discretionary annual bonus • Health insurance • Retirement savings benefits • Life insurance • Disability benefits • Parental leave • Paid time off for sick leave and vacation

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume