Site Contracts Manager

🔥 19 hours ago

🌐 Poland, Slovakia, +4 more countries – Remote

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

💵 zł190.2k - zł237.8k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 10%

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 services agreements, site contracts, consulting agreements, vendor agreements, clinical study agreements, amendments 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 and archiving of contract files and databases • Assist in designing and implementing procedures for timely contract execution • Identify process improvement opportunities and take corrective action • Work closely with Clinical Operations study teams to align deliverables with study timelines • Perform other assigned tasks

🎯 Requirements

• Graduate, postgraduate, 4-year college degree • Experience in a CRO/healthcare field • Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations, but no less than 5 years’ experience • Experienced leading interactions with Study Teams and Sponsor • Proficient in MS Office software programs and computer applications • Knowledgeable on setting up Contracting Plans - Guides for CTA & Budget negotiations • Successful handling relationship study team and/or with CRAs/Start-up Associate/(S)BSCA to meet study timelines • Strong organizational and written communication skills; ability to multi-task and prioritize in a fast-paced environment • Ability to execute time-sensitive matters while maintaining accuracy and attention to detail • Ability to work and plan independently and in a team environment • Sound business judgment and proactive, independent work style • Ability to handle sensitive issues with discretion • Ability to work cooperatively in a virtual environment