Feasibility Specialist (Associate) - Spain - FSP

If you want to be part of a leading CRO and transform scientific discoveries into new treatments, then Parexel FSP challenges you to live up to your potential by joining us at Feasibility Specialist (Associate) , home-based and sponsor dedicated, in Spain.

In this role you will be responsible for supporting feasibility processes for clinical trials. This role involves conducting research and data analysis to identify potential Clinical Trial Investigators and sites, ensuring data accuracy in clinical systems, and collaborating with various internal stakeholders to assist in optimizing study design and execution. The Feasibility specialist will engage with clinical trial sites/Investigators to gather feasibility surveys or additional requested data and ensure accurate and comprehensive responses.

We are looking for hard-working, talented, high-caliber people. We know that employee satisfaction leads to customer satisfaction, which is the ultimate driver of long-term success.

As the company that conducts vital clinical studies for sponsors, including the world's leading biotech’s and top 50 pharmaceutical companies, we offer you enormous security and long-term prospects.

You will work from your home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.

The most significant aspect of this position is

• Supporting the Feasibility, Strategy, & Analytics Lead (FSAL) to ensure knowledge of the goals, scope and requirements of a Site Feasibility project, and ensures that high quality insights are delivered  

• Clinical Systems Support: Administer and maintain clinical trial management systems (CTMS) and other relevant Feasibility tools  

• Data Analysis: Perform research and data analysis to identify suitable clinical trial sites.  

• Feasibility Activities: Assist with the setup of feasibility studies, including outreach to potential sites. 

• Stakeholder Coordination: Communicate and coordinate with FSAL, site staff, and other stakeholders to support feasibility efforts  

• Troubleshooting: Address and resolve any issues or discrepancies in the feasibility process as they arise or as directed 

• Acts as a supportive team member for Regional Intelligence  

• Performs tasks for multiple Site Intelligence and Feasibility projects.  

• Able to manage multiple volume of studies and sites 

• Works under close supervision of Regional Intelligence Team Lead, and where needed the Feasibility Specialist Point of Contact (POC) or more experienced colleagues  

• Contributes to executing Site Feasibility plans and presenting the data to colleagues. 

• Supports the Feasibility Strategy & Analytics Lead (FSAL) to ensure knowledge of the goals, scope and requirements of a Site Feasibility project, and ensures that high quality results are delivered.   

• Applies skills and discipline knowledge to OARS and Regional Intelligence development projects, when proficiency in role has been mastered  

• Promotes a continuous improvement culture to streamline appropriate processes for maximum efficiency and productivity 

• Develops and maintains internal processes aimed to optimize country & site selection activities 

• Creates awareness by working as a cross functional team leader to deliver data, analytics and regional site intelligence initiatives across a broad spectrum of stakeholders, both internal and external  

• Runs operational and technical aspects of large global projects and assists with other Company systems activities related to site intelligence 

• Maintains effective relationships with other platform lines, Business Units/Research Units, and enabling lines that facilitates effective portfolio delivery 

• Partners with GSSO and CD&O teams to improve overall study start up metrics and implement simple processes  
  

From you we expect

• At least 2 years of experience in feasibility in Clinical Research/Clinical Operations. Looking for candidates who worked previously asCountry Approval Specialist or Clinical Trial Coordinator or Site Relationship Coordinator.

• Multilingual: Fluent spoken and written abilities in local language in addition to English (e.g. French, Spanish, German, Mandarin etc.)  

• Effective verbal and written communication skills in relating to colleagues and stakeholders both inside and outside of the organization  

• Strong presentation skills, interpersonal skills, as well as a team oriented approach. Excellent verbal, written, communication and time management skills  

• Ability to multitask under tight deadlines on several projects with specific and unique requirements, while providing attention to detail and high quality work 

• Experience in a clinical research organization and related therapeutic specialties with familiarity in principles, concepts, practices and standards.  

• Experience working in the pharmaceutical industry or CRO or at site in a similar role.

• An eye for detail and ability to problem solve operational challenges and provide high level insights to a multidisciplinary team.  

• Proficiency in Microsoft SharePoint  

• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, database applications)  

• A quick learner with the desire to contribute and support the design and implementation of analytical insights and management of data platforms.  

• Demonstrated success/results in prior roles including matrix

  organization.

For an immediate interview, please contact marta.kuniewicz@parexel.com