Senior Project Manager

🕒 October 8

🇺🇸 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: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

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

Upload Resume

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 to meet quality, scope, cost and time objectives • Serve as primary point of contact and escalation point for clients • Coordinate and oversee functional services and external vendors against timelines and budgets • Manage study budgets, scope, out-of-scope activities, financial health, profitability, billable hours, billing and forecasting • Collaborate with clinical operations and functional teams in study delivery and clinical activities • Develop comprehensive project plans, timelines and proactive risk mitigation strategies • Ensure project quality, eTMF inspection readiness, quality notifications and corrective/preventive action plans • Establish tracking metrics for trial and team progress • Prepare project status updates and report KPIs and progress to clients and senior management • Lead internal and client meetings and set project-team expectations • Communicate protocol and study issues, deviations and required 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 to effectively interface with others in a team setting • Proven organizational skills, attention to detail, and a customer service demeanor • Knowledge of ICH-GCP and relevant Precision SOPs, with ability to implement them • 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 awareness of appropriate escalation • Proven experience in strategic planning, risk management and change management • High level of integrity and professional and ethical standards • Ability to lead and inspire excellence within a study team • Proven time management, negotiation, critical thinking, decision-making, analytical and interpersonal skills • Proven presentation, verbal and written communication skills • Good understanding of project management software • In-depth proven experience in pharmaceutical and/or device research required • 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