Senior Clinical Research Associate

BeiGene, Ltd.; Toronto; On-site; CAD 80,000 - 100,000; Full time

Job summary

A global oncology company is seeking a Senior Clinical Research Associate in Toronto. This role involves managing clinical study sites to ensure data quality and patient safety. The ideal candidate will have 4-6 years of relevant clinical operations experience and a strong understanding of clinical trial processes. This position offers full-time employment with significant responsibilities and the opportunity for mentorship within a collaborative environment.

Qualifications

• 4-6 years of relevant Clinical Operations experience.
• 3-4 years of CRA monitoring experience in the pharmaceutical or CRO Industry.
• Understanding of clinical trial processes and ICH guidelines.

Responsibilities

• Perform clinical monitoring in accordance with GCPs and SOPs.
• Conduct site visits for compliance checks.
• Develop collaborative relationships with study sites.

Skills

Excellent communication skills

Organizational skills

Interpersonal skills

Analytical thinking

Education

BS / BA in a relevant scientific discipline

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Microsoft Outlook

Job description

Senior Clinical Research Associate page is loaded

Senior Clinical Research Associate

Apply locations Toronto time type Full time posted on Posted Yesterday job requisition id R30833

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description :

The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.

The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other CRA team members within established protocols and portfolio under general supervision.

Proactively seeks opportunities to lead and drive improvements to optimize effectiveness and efficiencies within the Site Management group as well as within the greater Americas region.

Essential Functions of the job :

• Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs to assess the safety and efficacy of investigational products and / or medical devices
• Conduct site visits to determine protocol and regulatory compliance, and prepare required documentation
• Develop collaborative relationships with investigative sites, and study vendors
• Track enrollment status reports to ensure study sites stay on track to meet enrollment goals
• Track study-specific status reports to ensure all required information regarding site issues, deviations, and CRF status are kept current by the monitoring team
• Serve as mentor / trainer for less experienced CRAs to assist with general and study-specific monitoring issues
• Provide direct support to the Clinical Study Manager by assisting with monitoring visit report review and other managerial tasks as needed
• Perform study-specific training with project team
• Develop study-specific monitoring tools and forms for use by monitoring team to assist in efficient review of study data
• Perform Serious Adverse Event (SAE) reconciliation and work with study sites and CRAs to resolve discrepancies
• Review outstanding data reports and work with CRAs to ensure data collection is met per contractual guidelines
• Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under general supervision
• Collaborates with CST and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.).
• Provide support for study sites, and CRAs with audits / inspections preparation / responses and quality issues, as needed, and follow-through with audit / inspection findings to resolution as it related to involved CRA staff.
• Assist with other assigned clinical responsibilities within scope of role to provide best practice and / or support to junior clinical staff.

Supervisory Responsibilities :

Provides site level management for established protocols and portfolio under general supervision

Provides mentoring / support to CRAs for study related topics

Identification of development opportunities and provides necessary training to for junior team members as needed

Co-monitoring with CRAs and support site visits, as needed

Computer Skills :

Efficient in Microsoft Word, Excel, PowerPoint and Outlook

Familiar with industry CTMS and data management systems

Other Qualifications :

Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines

Minimum of 4-6 years of relevant Clinical Operations experience

Minimum of 3-4 years of (CRA) monitoring experience in the pharmaceutical or CRO Industry

Excellent communication and interpersonal skills

Excellent organizational skills and ability to prioritize and multi-task

Travel : up to 40-60% time

Education Required :

BS / BA in a relevant scientific discipline and minimum of 4-6 years of relevant Clinical Operations experience, and minimum of 3-4 years of monitoring experience. Experience in global oncology trials preferred.

Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

Fosters Teamwork

Provides and Solicits Honest and Actionable Feedback

Self-Awareness

Acts Inclusively

Demonstrates Initiative

Entrepreneurial Mindset

Continuous Learning

Embraces Change

Results-Oriented

Analytical Thinking / Data Analysis

Financial Excellence

Communicates with Clarity

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

About Us

BeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 11,000 colleagues spans six continents. To learn more aboutBeOne, please visitwww.beigene.com and follow us onLinkedIn ,X (formerly known as Twitter),Facebook andInstagram .

To Mainland China Candidates

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At BeOne, how we work is just as important as the work we do . Below are our Values that determine the decisions we make and how we do things.

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