The Site Feasibility Liaison is a key role for the delivery of Parexel studies. Site selection is challenging but is the cornerstone of more predictable recruitment. Better site selection requires excellent working relationships with institutions, investigators and research teams and better data organization to improve efficiency and knowledge.

****MANDATORY - PORTUGUESE FLUENCY REQUIRED****

The Site Feasibility Liaison will build effective relationships with Investigators and research sites and will champion Parexel within their region.

The Site Feasibility Liaison will be a local, clinical expert to represent their country/region. They will be advocates for their region to ensure it is included in the Parexel portfolio and support new business opportunities by helping to gather critical data to support client meetings or deliverables. They will be experts in terms of local infrastructure, standards of care, healthcare trends and guidelines.

The Site Feasibility Liaison, in conjunction with site intelligence and site alliance teams, will work to improve the knowledge that we have on clinical research teams and facilities. This will include owning the quality of information within the new Parexel Investigator Intelligence Platform that pertains to their country, region or therapeutic area.

What you will do in this dedicated role within the Global Feasibility team:

Input local expertise to the site selection process for Parexel projects:

Review draft site lists, communicate with sites to ensure high response rates, coordinate CDA collection – if necessary, query inconsistent/incomplete survey information, provide data-driven recommendations with regards to site selection Conduct phone interviews/follow-up with Investigators or site personnel to discuss standard of care, trends, patient barriers, protocol design considerations.

Local Clinical Expert:

Support the central feasibility teams with local insight to support country strategy, protocol development and new business awards. Provide accurate, timely and realistic information. Proactively work to understand healthcare re-imbursement, trial infrastructure, patient motivations, patient support groups, site networks, new potential sites/Investigators for consideration in your country, region, therapy area Understand, communicate, and help to mitigate the risks to delivery for your country, region, therapy area.

Data Stewardship:

Proactively work to ensure accuracy of critical information held in the Investigator Intelligence Platform relevant to your country, region or therapy area. Work to build out valuable profile information for key sites to improve efficiency and improve the site experience.

Network & Collaboration:

Actively work with clinical and medical experts in your country to promote collaboration and to facilitate information gathering. Work closely with central feasibility counterparts to ensure a common understanding of risk and to promote the consideration of your country or region in future trials. Develop and maintain collaborative relationships with Investigators and site personnel Encourage and promote a culture of innovation and respect with the patient first and foremost.

Desired skillset:

• Autonomous, driven, someone who takes pride in quality of work with attention to detail

• Able to build effective relationships with others (Investigators, research teams) with a strong client focus

• Exceptional interpersonal, communication, analytical, problem-solving skills.

• Capable to work in a matrixed environment, valuing the importance of teamwork.

• Ability to be flexible and ability to manage multiple tasks effectively.