Clinical Trial Liaison - Contractor - Oncology - Europe - Remote

Worldwide Clinical Trials; Poland; Remote; PLN 255,000 - 341,000; Full time

Job summary

A global clinical research organization is seeking a Clinical Research Expert to manage relationships with key opinion leaders and support clinical trials in Poland. The ideal candidate will have a doctoral degree and over 5 years of experience in clinical research, particularly in solid tumors and melanoma. Strong networking and communication skills are crucial for success in this role, which offers an inclusive environment for diverse talents.

Qualifications

• Minimum of 5 years experience in clinical research.
• Minimum of 3 years experience in the assigned therapeutic area.
• Demonstrated experience of working directly with clinical sites.

Responsibilities

• Establish and maintain relationships with key opinion leaders.
• Conduct targeted conversations with investigators about operational challenges.
• Support project teams with site identification and selection.

Skills

Networking skills

Written and verbal communication skills

Negotiation skills

Problem-solving skills

Critical thinking

Operational expertise

Experience in solid tumor and melanoma

Education

Doctoral degree

Job description

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.

What the Scientific Solutions Department does at Worldwide

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.

What you will do

• 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.

What you will bring to the role

• 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 solid tumor and melanoma

Your experience

• 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

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity.