Clinical Trial Liaison

This is a fully remote position, open to applicants in California, +1 more state.

📋 Description

• Develop and maintain peer-to-peer relationships with Principal Investigators, site staff, key opinion leaders, sub-investigators, and healthcare providers in the fields of Neuroscience and Oncology.

• Act as a field-based expert in scientific and clinical trials, serving as an advocate.

• Facilitate protocol discussions with Principal Investigators and clinical site personnel.

• Direct site engagement strategies to enhance trial performance and site operations.

• Recognize obstacles to patient screening, enrollment, and retention.

• Collaborate with cross-functional stakeholders and CRO partners to design and implement territory plans.

• Relay clinical and research insights and issues to clinical study teams.

• Engage in educational activities regarding clinical studies for healthcare professionals.

• Assist sites with on-site presentations at healthcare institutions, conferences, and local communities.

• Offer scientific support for site and patient engagement initiatives as well as study-specific materials.

• Record and submit reports on adverse events and product complaints.

• Comply with relevant national and local Codes of Practice.

⛳️ Requirements

• Advanced degree (PharmD, MD, PhD, or equivalent) with at least 3 years of experience in oncology and/or neuroscience 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 and/or neuroscience medicine.

• At least 2 years of experience as a Medical Scientific Liaison (MSL), Clinical Scientist, Clinical Trial Liaison (CTL), or a similar field-based industry or clinical role.

• Strong grasp of clinical trial methodology, GCP, the overall drug development process, and regulatory requirements.

• Familiarity with regulatory and legal requirements for field-based personnel interacting with healthcare professionals.

• Excellent proficiency in written and spoken English.

• Strong skills in utilizing digital platforms and tools.

• Knowledge of relevant geographies, healthcare environments, and connections with external experts in academia and medical communities.

• Well-established network and capability to build trust and relationships with opinion leaders, Principal Investigators, clinical trial networks, and site research personnel.

• Willingness to work outside standard business hours.

• Availability to travel up to 60% of the time.

• Possession of a valid driver’s license and residence near a major airport.

• A strong track record in the targeted therapy areas and indications is highly preferred.

🏝️ Benefits

• Discretionary annual cash bonus or incentive compensation.

• Discretionary equity grants.

• Medical insurance.

• Dental insurance.

• Vision insurance.

• 401k retirement savings plan.

• Flexible paid vacation.