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Study Start-Up Specialist

Role overview

Summary

This role focuses on supporting study start-up processes and ensuring compliance with regulations and timelines. BeOne seeks a professional to enhance site activation efficiency and improve submission quality, contributing to the company's mission in the clinical research sector.

Qualifications

  • Minimum of 2 years of progressive experience in clinical research and clinical operations.
  • Familiarity with ICH/GCP and relevant country regulations/guidelines.
  • Skilled in document management and negotiation.
  • Preferred: Bachelor’s degree or higher in a scientific or healthcare discipline
  • Preferred: Experience within the biotech, pharmaceutical sector, CRO, or clinical site environment

Responsibilities

  • Support in the delivery of study start-up and ongoing submissions within established timelines.
  • Contribute to discussions during the feasibility stage of site selection.
  • Drive kick-off and completion of tasks from selection through activation.
  • Manage document preparation and submission to central IRB for timely reviews.

Key facts

Hard skills

Other skills

  • Timelines
  • Teamwork
  • Self-Awareness
  • Analytical Thinking
  • Communication

About the company

BeOne Medicines logo

BeOne Medicines

  • Pharmaceuticals
  • 10,001+
BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting the development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.

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Job description

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:

Support in the delivery of study start-up, initial and ongoing submissions within established timelines with high quality and in accordance with ICH/GCP, BeiGene SOPs, and local regulations.

Essential Functions of the job:

Familiar with ICH/GCP, relevant country regulations/guidelines, and SOPs

Contribute to discussions during the feasibility state of site selection

Site Start-Up

  • Skilled in driving kick-off and completion of tasks from selection through activation, including providing timeline input for site activations.
  • Leverage and build upon existing site partnership data to execute start-up efficiently, reducing cycle times wherever possible.

ICF/Submissions

  • Skilled in document management/negotiation and leveraging site relationships to achieve submission targets from start-up through close-out.
  • Skilled in document preparation and submission to central IRB to ensure timely reviews.

Support in the collection and review of essential documents

Complete SSU data entry in CTMS

Complete timely and quality eTMF filing

Support in the development of local workflows to streamline output and deliverables

Contribute to the ongoing improvement of SSU infrastructure in North America

Perform additional tasks as assigned or required to achieve project, functional, departmental, or corporate goals

Supervisory Responsibilities: 

Not applicable

Education/Experience Required:

Bachelor’s degree or higher degree in a scientific or healthcare discipline preferred with minimum of 2 years of progressive experience in clinical research and clinical operations preferably within the biotech, pharmaceutical sector, CRO, or clinical site environment.

Salary Range Canada:

·         69,100,000.00 CAD -86,400.00 CAD

Please note that this job posting is being advertised to fill a budgeted position.

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.

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