[Hiring] Senior Clinical Trial Liaison - Oncology @Worldwide Clinical Trials

Role Description

Our Scientific Solutions team are highly valued within Worldwide! You are part of a team of experts who we count on to guide our sponsors and internal teams with strategic direction and support critical decision making within the sales and delivery phases of a clinical trial/program. In this role we will rely on you to support us with providing protocol considerations, regulatory strategy, guiding on country/site selection, site and patient engagement strategies, and other clinical trial delivery and drug development strategies as applicable.

• Establish and maintain relationships with key opinion leaders, sites, and their staff.
• Conduct targeted conversations with the investigators and site staff regarding operational challenges, including but not limited to those related to patient recruitment and retention.
• Have clinical and scientific discussions with investigators to ensure overall quality of study endpoints, including but not limited to understanding of clinical protocols, study feasibility, and enrolment and retention of appropriate trial participants.
• Convey KOL and site staff feedback and insight to internal and external teams.
• Support and guide project teams with site identification and selection based on knowledge of site capabilities and anticipated protocol challenges.
• Support business development activities through engagement with existing and prospective clients. Provide scientific and operational input on proposals in development; attend and present at bid defense meetings.

Qualifications

• Excellent networking skills to represent Worldwide with key local stakeholders.
• Excellent written and verbal communication skills - able to interact with physicians and all levels of internal and external management.
• Excellent negotiation, influencing and problem-solving skills.
• Self-motivated with proactive issue monitoring and management including risk assessment and contingency planning.
• Possess a combination of critical thinking and operational expertise and efficiency.
• Strong background and experience in oncology studies.

Requirements

• A doctoral degree is required.
• Minimum of 5 years’ experience in clinical research in academia, Pharma, Biotech or CRO, including background in operational aspects of clinical research.
• Minimum of 3 years’ experience in the therapeutic area/indication assigned.
• Demonstrated experience of working directly with clinical sites and investigators.

Benefits

• We love knowing that someone is going to have a better life because of the work we do.