Site Contracts Manager

🔥 0 minutes ago

🌐 Romania, Poland, +3 more countries – Remote

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

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 10%

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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 • 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 • Bachelors in law, scientific fields, business administration or equivalent degree (Preferred) • Excellent organizational and communication skills and attention to detail (Preferred) • Knowledgeable on setting up Contracting Plans - Guides for CTA & Budget negotiations (Preferred) • Successful handling relationship study team and/or with CRAs/Start-up Associate/(S)BSCA to meet study timelines (Preferred) • Strong organizational and written communication skills; ability to multi-task and prioritize • Ability to execute time-sensitive matters accurately and with attention to detail • Ability to work independently and in a team environment • Proficiency in MS Office software programs and computer applications • Ability to handle sensitive issues with discretion • Ability to work cooperatively in a virtual environment