Site Feasibility Liaison

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

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.

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.

This is a dedicated role within the Global Feasibility team and is part of our Global Feasibility Network.

Key Accountabilities:

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 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.

Provide input on sites’ previous trial performance in similar indications, highlight fast starter sites that can be initiated within up to 3 months

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.

Update the TMF system for recommended sites to support timely CRA resource assignment.

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.

• Exceptional analytical and problem-solving skills

• Effective interpersonal, presentation, oral and written communication skills

• Capability to work in a matrix environment and to value the importance of teamwork.

• Ability to manage multiple tasks, to be flexible and to prioritize

• Sense of urgency to respond to client requests

• Strong computer skills

Knowledge and Experience:

• Several years Pharmaceutical/CRO Industry Experience in Clinical Research

• Multiple years in clinical management/feasibility management of global clinical trials with significant local clinical experience

• Demonstratable understanding and experience in selecting and starting up clinical trial sites

Education:

• Degree / further degree. MSc, MBA, Ph.D. or equivalent preferred

• Scientific/Medical/Nursing background

Language Skills

• Fluent in English, oral and writte