Sr Start-up Manager

ICON Strategic Solutions; Burlington; On-site; CAD 90,000 - 130,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance

Retirement planning

Global EAP (LifeWorks)

Life assurance

Country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Start-Up Manager in Canada to lead country-level study start-up activities in compliance with ICH-GCP and local regulations. You will prepare regulatory documentation, manage submissions, and collaborate with CRAs to ensure timely milestones.

The role requires a life sciences degree and 5+ years in Clinical Research focusing on Start-Up, with strong project management and communication skills. Competitive benefits and global exposure are offered.

Qualifications

• Bachelor’s degree in life sciences or related field.
• Minimum of 5 years of experience in Clinical Research, Start-Up focus.
• Strong project management with regulatory submission expertise.
• Excellent written and verbal communication abilities.
• Proven ability to meet tight deadlines and manage multiple priorities.

Responsibilities

• Lead start-up activities at country level in compliance with guidelines (ICH-GCP, regulations).
• Prepare, review, track and manage site regulatory documentation; maintain site performance metrics.
• Collaborate with CRAs and Local Study Team to achieve milestones.
• Contribute to feasibility assessments and quality in study start-up processes.
• Manage document collection, submission to Regulatory Authorities/IEC/IRB during start-up.
• Maintain CTMS/eTMF data per timelines and perform follow-ups to resolve outstanding actions.
• Provide regular updates to Line Managers on study milestones and issues.

Skills

Project management

Regulatory submissions

Communication

Time management

Clinical Research

Education

Bachelor’s Degree in Life Sciences

Tools

CTMS

eTMF

Job description

Start-Up Manager

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.

What You Will Be Doing

• The Study Start-up/Site Activation Lead is responsible at country level for managing and conducting start-up activities in compliance with the client procedures, documents, local and international guidelines such as ICH – GCP and relevant regulations.
• The Study Start-up/Site Activation Lead will prepare, review, track and manage site regulatory documentation at country and site level, and will maintain, review and report on site performance metrics.
• The Study Start-up/Site Activation Lead works in close collaboration with the CRAs and the Local Study Team/Local Study Associate Director to ensure that study start-up activities and milestones are achieved in a timely and efficient manner
• Typical Accountabilities:
• Contribute to ensure that clinical and operational feasibility assessment of potential studies is performed to the highest quality.
• Accountable for study start-up and regulatory maintenance being in charge with collection, preparation, review and tracking of documents for the application process;
• Accountable for submission of proper application/documents to Regulatory Authorities and/or IEC/IRB during start-up period.
• Actively participates in Local Study Team (LST) meetings.
• Update CTMS and other systems with data from study sites as per required timelines during the start-up period.
• Follow up on outstanding actions with study sites during start-up period to ensure resolution in a timely manner.
• Ensure timely collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, client SOPs and local requirements. Support QC checks performed by Trial Manager or delegate to ensure that all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enroll, and in line with client SOPs.
• Provide regular information to Line Managers at country level on study and planned study milestones/key issues during the start-up period.

Your profile

• Bachelor’s Degree, preferably in life sciences.
• Minimum of 5 years of experience in a Clinical Research environment, focusing on Start-Up.
• Strong project management skills, with a deep understanding of regulatory and submission processes
• Excellent written and verbal communication abilities.
• Proven ability to work efficiently to tight deadlines and manage multiple priorities.

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.