Clinical Development Consultant - Site Engagement Liaison (Greater Toronto Area)

ICON Strategic Solutions; Toronto; On-site; CAD 70,000 - 110,000; Full time

Job summary

Join a leading clinical research organization as a Clinical Development Consultant, where you will play a pivotal role in managing clinical trial sites. This position involves overseeing site identification, qualification, and ensuring timely enrollment in clinical trials. You will be the key communication link between sites and vendors, developing strong professional relationships with clinical investigators. If you are passionate about making a difference in clinical research and thrive in a dynamic environment, this opportunity is perfect for you. Embrace the chance to contribute to innovative healthcare solutions while advancing your career in a supportive and collaborative setting.

Qualifications

• Experience in managing clinical sites and ensuring trial enrollment.
• Strong skills in vendor oversight and issue resolution.

Responsibilities

• Manage clinical sites, ensuring timely enrollment and inspection readiness.
• Develop strategic relationships with investigators and site staff.

Skills

Clinical Trial Management

Vendor Oversight

Risk Management

Relationship Building

Communication Skills

Education

Bachelor’s Degree in Life Sciences

Master’s Degree in a related field

Job description

As a Clinical Development Consultant (site engagement) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities:

The Clinical Research Lead is responsible for the management of clinical sites including the site identification and qualification, the timely delivery of clinical trial enrollment in accordance with scientific objectives, timely delivery of database locks, issues management at clinical trial sites, and ensuring inspection readiness at all times for assigned therapeutic areas within a region or country. You will also be responsible for the oversight of vendor monitoring activities at clinical trial sites, including the identification, mitigation and escalation of significant findings and trends.

Key Responsibilities:

• You will be responsible for all activities required at clinical trial sites and by investigators and site staff participating in the client’s trials; including the site identification and qualification, enrollment planning and execution, to database lock and close out.
• You will also perform management and issue mitigation, identification and resolution.
• The development of strategic institutional/site relationships will be a main focus.
• You will develop and implement site risk plans, ensure site and country level inspection readiness at all times, leverage metrics to inform site/country/regional level for their decision making and provide vendor oversight for site monitoring activities at site/country level.
• It will be a goal to establish and develop strong professional relationships with clinical investigators.
• All in all you will be the communication “bridge” between sites, third party vendors and the client.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Research, Analyst, and Science

Industries

• Pharmaceutical Manufacturing