Site Contracts Manager

🔥 0 minutes ago

🌐 Slovakia, Poland, +3 more countries – Remote

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

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 20%

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 confidentiality agreements, master confidentiality agreements, clinical study agreements and amendment agreements • Review, draft and negotiate master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality 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 • Maintain contract files and databases, including contract archiving • Assist in designing and implementing procedures for timely contract execution • Identify process improvements and take corrective action • Collaborate with Clinical Operations study teams to align deliverables with study timelines

🎯 Requirements

• Graduate, postgraduate, 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 Sponsor • Preferred: Bachelor’s degree in law, scientific fields, business administration or equivalent degree • Knowledge of Contracting Plans and guides for CTA and budget negotiations • Proficiency in MS Office software programs and computer applications • Ability to work independently and cooperatively in a virtual environment • Strong organizational, written communication, multitasking and prioritization skills • Ability to handle sensitive issues with discretion • Must be legally authorized to work in the country of employment without employer sponsorship

🏖️ Benefits

• Fully remote work arrangement • Equal opportunity employment • Reasonable accommodation during the application process