Demo

Site Partner Engagement Specialist

Lifelancer
Madison, WI Full Time
POSTED ON 2/16/2025
AVAILABLE BEFORE 5/9/2025

Job Title : Site Partner Engagement Specialist

Job Location : Madison WI USA

Job Location Type : Remote

Job Contract Type : Fulltime

Job Seniority Level : Entry level

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient access and technology solutions across more than 20 therapeutic areas. Conducting operations in 100 countries Fortrea is transforming drug and device development for partners and patients across the globe.

Fortrea is one of the largest earlystage clinical research organizations in the world. Our Clinical Pharmacology Services team helps clients to introduce their compound in humans and move to proofofconcept. Our customers depend on us to generate critical data that determine the future of investigational drugs. It might be a tube of blood that is destined for analysis of drug levels or an ECG to examine the QT interval… much of the data we generate ends up in a drug’s label!

YOUR MISSION

Clinical Pharmacology studies have grown in complexity. As Fortrea is being entrusted to deliver more sophisticated study protocols and move towards bigger multi country / multi center studies the industry is experiencing increased challenges to access unique capabilities and per protocol volunteers and patient populations.

We Have Nurtured a Relationship With a Vast Network Of External Sites / Investigators Around The Globe But To Succeed In This Complexity We Must Expand And Create Synergetic Relationships And Quality Oversights With Our External Site Network. This Is Why We Need You To

  • Identify the top performing high quality external site partners globally to deliver our client´s protocol with minimum risks
  • Build strong relationships with these partner´s collecting detailed capability experience and quality metrics in support of the site’s operational success mitigating risk to study conduct for Fortrea sponsors and
  • Actively manage the network database and file repository in support of the Fortrea External Site Governance Model

What You Will Do Day To Day

  • Accountable for the growth and maintenance of the CPS external site network and documentation databases supporting data collection analysis and presentation of key metrics for implementation of external site strategies for CPS clinical trials.
  • Obtain enter and maintain data for quality correctness and context for Requests for Information / Proposal (RFIs / RFPs) Bid Defense Meetings (BDMs) client calls capabilities presentations external site qualification and feasibility analysis audit history etc.
  • Maintain enter and generate reports related to external site partners as per Fortrea External Site Governance Model.
  • Generate preliminary site lists for both early and late phase study trials in response to queries for site identification
  • Assist in the feasibility assessment and development of strategic study plans by providing relevant site data in response to pre and postaward study deliverables RFIs / RFPs BDMs client calls capabilities presentations site governance and escalation or investigations etc.
  • Leverage CPS tools to generate data in support of :
  • Geographical location of fit
  • Site Experience and expertise
  • Enrollment metrics
  • Who Will You Work With

    Your team is split between the UK and the US. You will interact daily with Clin Ops teams PMs Startup and external sites; and also with global crossfunctional teams that plan analyze and implement solutions to drive new business initiatives.

    Qualifications

    WHAT YOU WILL BRING :

  • A university / college degree or equivalent experience in lieu of education
  • 12 years’ experience in site qualification or feasibility and understanding of global drug development and clinical trials.
  • Knowing the nuances of Phase 11b clinical trials is a plus
  • Work Experience

  • Excellent computer skills including strong working knowledge of Microsoft Office Microsoft SharePoint and other data capture and compilation tools. Ability to understand and leverage technology alternatives
  • Knowledge of data analytics and associated tools
  • Strong affinity for numbers data large amounts of information
  • High attention to detail / quality control skills
  • Strong data mining and analytical skills with the abilities to review / analyze relevant data to assist in building solution driven clinical trial strategies
  • Pay Range : $60000 – 90000 / year

    Benefits : All job offers will be based on a candidate’s skills and prior relevant experience applicable degrees / certifications as well as internal equity and market data. Regular fulltime or parttime employees working 20 or more hours per week are eligible for comprehensive benefits including : Medical Dental Vision Life STD / LTD 401(K) Paid time off (PTO) or Flexible time off (FTO).

    Application Deadline Date : February 21 2025

    Fortrea is actively seeking motivated problemsolvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process ensuring the swift delivery of lifechanging ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured enabling you to make a meaningful global impact. For more information about Fortrea visit

    Fortrea Is Proud To Be An Equal Opportunity Employer

    As an EOE / AA employer Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race religion color national origin gender (including pregnancy or other medical conditions / needs) family or parental status marital civil union or domestic partnership status sexual orientation gender identity gender expression personal appearance age veteran status disability genetic information or any other legally protected characteristic. We encourage all to apply.

    For more information about how we collect and store your personal data please see our Privacy Statement.

    If as a result of a disability you require a reasonable accommodation to complete your job application preemployment testing job interview or to otherwise participate in the hiring process please contact : . Please note that this email address is only for job seekers requesting an accommodation. Please do not use this email to check the status of your application.

    Lifelancer ( ) is a talenthiring platform in Life Sciences Pharma and IT. The platform connects talent with opportunities in pharma biotech health sciences healthtech and IT domains.

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    Key Skills

    Internship,Data Warehousing,Adobe Flash,Database Administration,Logistics

    Employment Type : Full Time

    Vacancy : 1

    Salary : $60,000 - $90,000

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