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CONTRACT SPECIALIST - FSP - POLAND

Thermofisher
Full-timemid

Job description

<p style="text-align:left"><b>Work Schedule</b></p>Standard (Mon-Fri)<p style="text-align:inherit"></p><p style="text-align:left"><b>Environmental Conditions</b></p>Office<p style="text-align:inherit"></p><p style="text-align:left"><b><u>Job Description</u></b></p><p style="text-align:inherit"></p><p>Join Us as a Site Contract Specialist – Make an Impact at the Forefront of Innovation<br />We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100&#43; countries in the last 5 years.<br /><br />As part of our global team, you’ll have the opportunity to prepare and negotiate contracts, as well as finalize the contract process. As a Site Contract Specialist, you&#39;ll liaise and establish effective relationships with sites and internal functional teams. You will ensure quality, objectivity, and risk analysis in the efficient delivery of contracts.<br /><br />What You’ll Do:</p><p>· Negotiate directly with assigned sites on all site related contracting items including clinical trial agreements, budgets, payment terms, ancillary agreements and amendments.</p><p>· Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&amp;C metrics and deliver processes.</p><p>· Ensure standards are applied to the SB&amp;C processes across projects.</p><p>· Leverage leading industry tools and data sources to provide budget and contract feedback aligned with parameters and fair market value guidance.</p><p>· Promptly recognize and improve potential delays and escalate to appropriate team members.</p><p>· Track all actions and negotiations to ensure timelines are achieved for studies and sites assigned.</p><p>· Support resolving escalated issues identified by the site activation sub-team in partnership with the internal Study Startup team.</p><p><br />Education and Experience Requirements:</p><p>· BSc degree or international equivalent</p><p>· 2 or more years of experience in clinical research site contracting and budgeting within a pharmaceutical company, CRO or relevant industry vendor.</p><p>· Ability to explain data to facilitate decision making processes to be data driven.</p><p>· Knowledge and understanding of clinical study protocols and schedule of assessments</p><p>· Strong organizational skills, decision making, communication and negotiation skills</p><p><br /><br />Working Conditions and Environment:<br />• Ability to work in an upright and /or stationary position for 6-8 hours per day.<br />• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.<br />• Frequent mobility required.<br />• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.<br />• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.<br />• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.<br />• Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.<br />• Frequently interacts with others to obtain or relate information to diverse groups.<br />• Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.<br />• Regular and consistent attendance.</p><p></p><p></p><p></p><p></p>