Clinical Trial Liaison FSP

Parexel are currently recruiting for an experienced Global Patient and Site Engagement – Clinical Trial Liaison professional to join one of our growing sponsors in Spain
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This will be a fully remote home-based position and is only open to applicants in the countries listed above.

• 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 Oncologytherapeutic area for select Jazz 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.
• Scientific Expertise
• Maintains an up to date anddeepknowledge of the therapy area,sponsor'sproducts, 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 the sponsor positioning as the scientific authority in Oncology.
• Acquiresa 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 andthe clinical experience with our products through scientific exchange and peer-to-peer interactions discussing benefits and risks in an objective manner.
• Provide scientific support foradditionalactivities such as medical congress staffing, advisory boards, and sales training initiatives
• 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 foradditionalactivities such as site and patient study specific material development.
• Share best practices across clinical trial teams and other functions.
• Consistently actstoenhancesponsor’s 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 eventsand product complaints according to sponsor’s policy to ensure safe and effective use of sponsor's products.
• Adheresto the relevant national and local Codes of Practice.
• Behaves ethically and with integrity at all times.
• Actsas an ambassador for sponsor's followingcompanymission and values.
  
  Keepsown written development plan and implements.
• Preparestimelyreporting according to the company needs.