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
Top Skills
What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
