Clinical Trial Liaison

Job not on LinkedIn

🔥 1 hour ago

🇪🇸 Spain – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Clinical Liaison

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Identify and develop peer-to-peer relationships with key opinion leaders, principal investigators, sub-investigators, and healthcare providers in Oncology for selected sponsor pipeline indications • Lead and drive site and patient engagement initiatives to improve clinical trial operational excellence, performance, patient experience, diversity, and inclusivity • Create and meet clinical operations objectives and work plans with cross-functional stakeholders, focusing on site and patient engagement, recruitment timelines, and deliverables • Maintain deep, current knowledge of the therapy area, sponsor products, emerging research, therapeutic issues, trends, and competitive landscape • Establish a reputation as a trusted source of scientific and medical information for the healthcare community • Support development of the sponsor’s positioning as a scientific authority in Oncology • Provide clinical presentations and scientific information in academic, community, and healthcare provider settings • Communicate emerging data and clinical experience through objective scientific exchange and peer-to-peer interactions • Provide scientific support for medical congress staffing, advisory boards, sales training initiatives, and study-specific material development • Develop and execute territory plans aligned with site engagement plans • Lead site and patient activities cross-functionally across the portfolio and resolve issues creatively • Identify and communicate clinical and research insights from clinical research sites and healthcare providers to clinical study teams • Participate in clinical study education for healthcare professionals and support sites through presentations at healthcare institutions and surrounding communities • Share best practices across clinical trial teams and functions • Enhance the sponsor’s image as an advocate of medical advancement through meaningful scientific exchange • Document and forward adverse event and product complaint reports according to sponsor policy • Adhere to relevant national and local Codes of Practice and act ethically and with integrity • Act as an ambassador for the sponsor’s mission and values • Prepare timely reporting according to company needs • Travel frequently between meeting sites and use computers, laptops, tablets, telephones, and similar equipment

🎯 Requirements

• Advanced degree (PharmD, MD, PhD or equivalent) with a minimum of 3 years of experience in oncology medicine, 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 • Minimum of 2 years of experience as a Medical Science Liaison or comparable industry or clinical role • Spanish is required • Willingness to travel approximately 60% of the time • Valid driver’s license • Live in proximity of a major airport • Ability to research, 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 able to work autonomously • Ability to learn quickly, be flexible, and remain results-focused in a rapidly changing environment • Excellent negotiation skills • Demonstrated interpersonal relationship building, networking, collaboration, and teamwork skills • Ability to influence without authority or gain acceptance/consensus in sensitive situations • Strong capabilities working with digital platforms and tools • Excellent command of spoken English • Knowledge of geography, healthcare environment, and external experts in academia and the medical community • Demonstrated ability to develop trust and relationships with opinion leaders in relevant disease states • Understanding of regulatory requirements for field-based personnel • Experience in solid tumors/targeted therapies and a strong track record of success strongly preferred

🏖️ Benefits

• Fully remote home-based position • Full-time employment • Professional development through maintaining and implementing an individual written development plan