GPSE- Clinical Trial Liaison- FSP

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.

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​ 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 

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​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.   

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​Required Knowledge, Skills, and Abilities 

​Required 

• ​Ability to research and critically analyze and communicate complex scientific and medical information and data. 
• ​Clear and concise communication and presentation skills. 
• ​Excellent planning and organization skills, with high-level attention to detail and accuracy. 
• ​Strong strategic mindset. 
• ​Highly self-motivated and ability to work autonomously. 
• ​Ability to learn quickly, be flexible and results-focused in a rapidly changing environment. 
• ​Excellent negotiation skills. 
• ​Demonstrated skills in inter-personal relationship building, networking, collaboration, and teamwork. 
• Requires the ability to influence without authority or gain acceptance/consensus from others in sensitive situations, without damage to the relationship.
• ​Strong capabilities working with digital platforms and tools are required.
• ​Excellent command of spoken English. 

Preferred 

• ​Knowledge of geography, healthcare environment and external experts in academia and medical community. 
• ​Demonstrated ability to develop trust and relationships with opinion leaders in disease states of interest. 
• ​Understanding of regulatory requirements for field-based personnel. 

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​Required/Preferred Education and Licenses

• ​Advanced degree (PharmD, MD, PhD or equivalent) with a minimum of 3 years of experience in oncology medicine is required, or  License (RN, NP, CNP, PA or equivalent) with a minimum of a Master’s Degree (or equivalent) and a minimum of 5 years’ experience in oncology medicine is required.
• A minimum of 2 years of experience as a MSL or comparable industry or clinical role is required.
• Experience in solid tumors/targeted therapies and a strong track record of success is strongly preferred. 
• This is a field position, and applicants must be willing to travel ~60% of time.
• Valid driver’s license and live in proximity of a major airport.

​Description of Physical Demands

• ​Frequent travel between meeting sites. 
• ​Frequently operating a computer, printer, telephone, and other similar office machinery. 

​Description of Work Environment

• ​Frequent interactions with external contacts in their office environment with little exposure to excessive noise, dust, fumes, vibrations, and temperature changes. 
• ​Frequent computer laptop or tablet use, not usually at a workstation. 
• ​Responsibilities may require a work schedule that may include working outside of “normal” work hours, in order to meet business demands. 
• ​Frequent public contact requiring appropriate business apparel.​

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EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.