Site Contracts Manager

🔥 13 hours ago

🌐 Slovakia, Poland, +4 more countries – Remote

🇸🇰 Slovakia – Remote 🇵🇱 Poland – Remote 🇪🇸 Spain – Remote 🇷🇸 Serbia – Remote 🇷🇴 Romania – Remote 🇭🇺 Hungary – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 19%

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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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

• Review, draft, negotiate, and track legal agreements, including confidentiality agreements, master confidentiality agreements, clinical study agreements, amendment agreements, master services agreements, site contracts, consulting agreements, vendor agreements, and other client contracts • Work with supervisors and internal/external stakeholders to resolve or escalate contractual issues • Ensure adherence to company policies, procedures, and contracting standards • Update study team members on contract negotiation and execution status • Establish, track, report, and manage site contract metrics • Support maintenance of contract files and databases, including contract archiving • Assist in designing and implementing policies and procedures for timely contract execution • Identify process improvements and take corrective action • Perform other assigned tasks

🎯 Requirements

• Graduate, postgraduate, or 4-year college degree • Experience in a CRO/healthcare field • At least 5 years of relevant experience drafting, reviewing, and negotiating site Clinical Trial Agreements, Vendor Contracts, and Site Budget negotiations • Experience leading interactions with Study Teams and Sponsors • Proficiency in MS Office software programs and computer applications • Strong organizational and written communication skills • Ability to multitask and prioritize in a fast-paced environment • Ability to execute time-sensitive matters accurately and with attention to detail • Ability to work independently and in a team environment • Ability to handle sensitive issues with discretion • Ability to work cooperatively in a virtual environment • Preferred: Bachelor's degree in law, scientific fields, business administration, or equivalent degree • Preferred: Knowledge of setting up Contracting Plans and guides for CTA and budget negotiations • Preferred: Successful relationship handling with study teams and/or CRAs/Start-up Associates/(S)BSCA

🏖️ Benefits

• Fully remote work arrangement • Regular full-time employment • Equal opportunity employment • Reasonable accommodation during the application process