Senior Clinical Project Research Manager

🕒 June 25

🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

👔 Manager

👻 Ghost score 45%

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.

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UBC

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2003

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

Healthcare • Consulting • Biotechnology

UBC is a company dedicated to improving patient outcomes by connecting specialty therapies to patients in need. They provide modern and customized solutions focusing on access, safety, and evidence generation for biopharmaceutical products. UBC specializes in evidence development, risk management, and patient access, utilizing real-world data and innovative technologies to optimize the healthcare journey and ensure effective medication use.

📋 Description

• Lead UBC project teams to deliver project milestones • Serve as the primary contact with the sponsor for all study related items • Oversight of all aspects of project conduct, from study start-up through close-out • Execute operational aspects of assigned project activities as well as special projects • Assist in the development and design of protocols, CRFs, regulatory documents, project master file, and other project related deliverables • Monitor project progress as compared to established plans and ensure compliance with plans • Facilitate and plan investigator meetings • Recruit qualified investigators and assist in budget negotiations as required • Supervise APM/PMs and other team members to ensure project deliverables and timelines are delivered accurately and timely • Provide reports to the Sponsor on project progress • Lead internal client teleconferences and/or meetings and present project information at client meetings • Maintain project documentation to be ‘audit ready’

🎯 Requirements

• 5 years of experience managing global clinical trials within the CRO industry • Observational study experience • Oncology experience is preferred • BA Degree or minimum 5 years of direct project management experience at a CRO or proven leadership/management experience • Excellent written verbal and non-verbal communication skills • Excellent supervisory skills • Excellent interpersonal skills • Excellent presentation skills • Ability to independently assess issues and/or mitigate risk by using critical judgment to come to a resolution • Solution driven • Manage competing priorities effectively • Very good knowledge of regulatory requirements (i.e. Good Clinical Practice, ICH guidelines, etc.) • 10% travel

🏖️ Benefits

• Remote opportunities • Competitive salaries • Growth opportunities for promotion • 401K with company match* • Tuition reimbursement • Flexible work environment • Discretionary PTO (Paid Time Off) • Paid Holidays • Employee assistance programs • Medical, Dental, and vision coverage • HSA/FSA • Telemedicine (Virtual doctor appointments) • Wellness program • Adoption assistance • Short term disability • Long term disability • Life insurance • Discount programs