Clinical Trial Liaison

About ParexelParexel is a leading global clinical development partner delivering insight-driven clinical and consulting solutions to the life sciences industry.
With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.
We work with focus, agility, and shared purpose, moving with urgency to address patient needs and accelerate the delivery of new therapies.
We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research.
We are expanding our team and seeking talented individuals to help drive industry-leading innovation, With Heart®.

About The Role
We are seeking a Global Patient and Site Engagement – Clinical Trial Liaison to join our team in Spain in a remote/home-based capacity.
This position offers the opportunity to contribute directly to the development of innovative therapies while building strong partnerships with sites and stakeholders.
Your work will help ensure that studies remain inspection-ready, compliant, and focused on delivering high-quality outcomes for patients.
You will join a collaborative, growth-oriented environment where your contributions are highly visible and where continuous learning, professional development, and meaningful impact are part of everyday work.

Key Responsibilities
Clinical Trial Site EngagementIdentify 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 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 ExpertiseMaintains an up to date and deep knowledge of the therapy area, sponsor's 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 the 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 initiativesDevelop 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.
Consistently act to enhance sponsor'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 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.
Always behaves ethically and with integrity.
Acts as an ambassador for sponsor's following company mission and values.
Keeps own written development plan and implements.
Prepare timely reporting according to the company needs.
Candidate ProfileYou'll Thrive In This Role If You BringAdvanc