Clinical Trial Liaison

This is a fully remote position, open to applicants in Spain.

📋 Description

• Identify and cultivate peer-to-peer relationships with key opinion leaders, principal investigators, sub-investigators, and healthcare providers in Oncology for designated sponsor pipeline indications.

• Lead and drive initiatives for site and patient engagement to enhance clinical trial operational excellence, performance, patient experience, diversity, and inclusivity.

• Create and fulfill clinical operations objectives and work plans with cross-functional stakeholders, concentrating on site and patient engagement, recruitment timelines, and deliverables.

• Maintain in-depth, up-to-date knowledge of the therapy area, sponsor products, emerging research, therapeutic challenges, trends, and the competitive landscape.

• Establish a reputation as a reliable source of scientific and medical information for the healthcare community.

• Assist in developing the sponsor’s positioning as a scientific authority in Oncology.

• Deliver clinical presentations and scientific information in academic, community, and healthcare provider environments.

• Communicate emerging data and clinical experiences through objective scientific exchanges and peer-to-peer interactions.

• Provide scientific support for medical congress staffing, advisory boards, sales training initiatives, and the development of study-specific materials.

• Formulate and implement territory plans that align with site engagement strategies.

• Lead site and patient activities across the portfolio and creatively resolve issues.

• Identify and relay clinical and research insights from clinical research sites and healthcare providers to clinical study teams.

• Participate in clinical study education for healthcare professionals and assist sites through presentations at healthcare institutions and surrounding communities.

• Share best practices among clinical trial teams and functions.

• Enhance the sponsor’s reputation as an advocate for medical advancement through meaningful scientific exchanges.

• Document and forward reports of adverse events and product complaints in accordance with sponsor policy.

• Comply with relevant national and local Codes of Practice and act ethically and with integrity.

• Serve as an ambassador for the sponsor’s mission and values.

• Prepare timely reports as per company requirements.

• Travel frequently between meeting sites and utilize computers, laptops, tablets, telephones, and similar equipment.

⛳️ Requirements

• Advanced degree (PharmD, MD, PhD or equivalent) with at least 3 years of experience in oncology medicine, or a license (RN, NP, CNP, PA or equivalent) with a minimum of a Master’s Degree (or equivalent) and at least 5 years of experience in oncology medicine.

• Minimum of 2 years of experience as a Medical Science Liaison or in a comparable industry or clinical role.

• Proficiency in Spanish is required.

• Willingness to travel approximately 60% of the time.

• Valid driver’s license.

• Reside near a major airport.

• Ability to research, critically analyze, and convey complex scientific and medical information and data.

• Clear and concise communication and presentation skills.

• Exceptional planning and organizational skills, with a strong focus on detail and accuracy.

• Strong strategic mindset.

• Highly self-motivated and capable of working independently.

• Ability to quickly learn, adapt, and focus on results in a rapidly evolving environment.

• Excellent negotiation skills.

• Proven ability to build interpersonal relationships, network, collaborate, and work effectively in a team.

• Capacity to influence without authority or achieve acceptance/consensus in sensitive situations.

• Strong skills in utilizing digital platforms and tools.

• Excellent command of spoken English.

• Familiarity with geography, the healthcare environment, and external experts in academia and the medical community.

• Proven ability to develop trust and relationships with opinion leaders in relevant disease states.

• Understanding of regulatory requirements for field-based personnel.

• Experience with solid tumors/targeted therapies and a strong record of success is strongly preferred.

🏝️ Benefits

• Fully remote home-based position.

• Full-time employment.

• Opportunities for professional development through the maintenance and implementation of an individual written development plan.