Site Activation Partner

Job summary

The Site Activation Partner facilitates clinical trial initiation by managing regulatory submissions and coordinating with stakeholders to obtain necessary approvals. They also support study teams in developing essential documentation such as protocols and informed consent forms.

Job details

Site Activation Partner - Canada At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Site Activation Partner at ICON, you will facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies. What You Will Do Your role will involve delivering site start-up and activation work to a high standard, working closely with your team and stakeholders. Key Responsibilities Include Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions. Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation. Maintaining accurate and up-to-date records of regulatory submissions and approvals. Supporting study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures. Participating in study start-up meetings and providing input on regulatory requirements and timelines. Your Profile You will bring relevant site start-up and activation experience, along with the following qualifications and skills. Required Qualifications And Experience Bachelor's degree in life sciences or a related field. Previous experience in clinical research or regulatory affairs preferred, but Nt required. Strong attention to detail and organizational skills. Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams. Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment. What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

What you’ll do

The Site Activation Partner facilitates clinical trial initiation by managing regulatory submissions and coordinating with stakeholders to obtain necessary approvals. They also support study teams in developing essential documentation such as protocols and informed consent forms.

Requirements

Candidates are required to hold a bachelor's degree in life sciences or a related field. Strong organizational skills, attention to detail, and the ability to manage multiple tasks in a fast-paced environment are essential.

Benefits

• Annual leave entitlements
• Health insurance
• Retirement planning
• Global Employee Assistance Programme
• Life assurance
• Childcare vouchers
• Bike purchase schemes
• Discounted gym memberships
• Subsidized travel passes
• Health assessments

Listed skills

• Regulatory Compliance · Preferred
• Attention to detail · Preferred
• Communication Skills · Preferred
• Cross-Functional Collaboration · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Clinical trials
• Regulatory affairs
• Site activation
• Regulatory submissions
• Ethics committee submissions
• Clinical trial applications
• Protocol development
• Informed consent forms
• Investigator brochures
• Stakeholder coordination
• Regulatory compliance
• Attention to detail
• Organizational skills
• Communication skills
• Cross-functional collaboration

Job areas

• Healthcare
• Science & Research
• Manufacturing

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