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 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 For Medicine

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $75M Private Equity Round on 2015-12

Healthcare • Consulting • Logistics

Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.

📋 Description

• Review, draft, negotiate and track legal agreements, including confidentiality agreements, master confidentiality agreements, clinical study agreements and amendments • 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 • Support maintenance and archiving of contract files and databases • Assist in designing and implementing procedures for timely contract execution • Identify process improvements 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 • 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 • Proficient in MS Office software programs and computer applications • 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 handling of relationships with study teams and/or CRAs/Start-up Associates/(S)BSCAs to meet study timelines • Strong organizational and written communication skills; ability to multitask and prioritize • 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

🏖️ Benefits

• Fully remote work arrangement • Equal Opportunity Employer • Reasonable accommodation available for the application process