GPSE- Clinical Trial Liaison- FSP

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.

Parexel FSP is looking for a GPSE (Global Patient and Site Engagement) – Clinical Trial Liaison.

This is a United States field position with applicants willing to travel approximately 60% of the time.

Essential Functions 

​Clinical Trial Site Engagement: 

• ​Identify and develop peer-to-peer relationships with key opinion leaders (KOLs), Principal investigators, sub-investigators, and healthcare providers within the Oncology therapeutic area for select Sponsor pipeline indications, including Breast Cancer, which are not currently covered by the Sponsor Medical Science Liaison (MSL) team, to lead and drive site engagement strategies.
• ​Lead and drive site and patient engagement initiatives to improve operational excellence and performance in the clinical trial program. Also, to enhance the patient experience in trials, to improve diversity and inclusivity of patients.
• Works with key stakeholders across functions to create and meet clinical operations objectives and work plans with emphasis on site and patient engagement, recruitment timelines and deliverables, and delegates assignments as appropriate.
• Develop and execute territory plans in alignment with site engagement plans.
• Lead site and patient activities cross functionally across the portfolio to achieve the group’s goals and objectives, resolving a wide range of issues in creative ways.
• ​Identify and communicate key clinical and research issues and insights from clinical research sites and healthcare providers to clinical study teams. 
• ​Participate in clinical study education for healthcare professionals (HCPs) in communities around clinical trial sites. Support sites through on-site presentations at healthcare institutions in local healthcare institutions and surrounding communities. 
• ​Provide scientific support for additional activities such as site and patient study specific material development.
• Share best practices across clinical trial teams and other functions.

​ 

​ Scientific Expertise

• ​Maintains an up to date and deep knowledge of the therapy area, Sponsor products, new and emerging areas of research, therapeutic issues and trends, and competitive landscape. 
• ​Establishes reputation as a trustworthy and knowledgeable source of scientific and medical information for the healthcare community.  
• ​Supports development of Sponsor positioning as the scientific authority in Oncology.
• ​Acquires a broad understanding of local and national protocols and standards of clinical practice and trends in disease management in the US.    
• ​Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic, community, and healthcare provider settings in both group and one-on-one situations.
• ​Communicates emerging data and the clinical experience with our products through scientific exchange and peer-to-peer interactions discussing benefits and risks in an objective manner. 
• Provide scientific support for additional activities such as medical congress staffing, advisory boards, and sales training initiatives 

​

​Embodies Sponsor Company Standards and Values  

• ​Consistently acts to enhance Sponsors’ image as an advocate of medical advancement by using knowledge of product, disease state and pipeline products to engage healthcare providers in meaningful scientific exchange of information.  
• ​Document and forward reports of adverse events and product complaints according to Sponsor’s policy to ensure safe and effective use of Sponsor's products.  
• ​Adheres to the relevant national and local Codes of Practice.   
• ​Behaves ethically and with integrity at all times.  
• ​Acts as an ambassador for Sponsor following company mission and values.   ​Keeps own written development plan and implements.   
• ​Prepares timely reporting according to the company needs.   

​ 

​Required Knowledge, Skills, and Abilities  

​Required 

• ​Ability to research and critically an