Study Start-up Specialist

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.

Job Description

PLEASE SUBMIT ALL RESUMES/CV'S IN ENGLISH FOR CONSIDERATION

Language Requirement: Fluent English required. Spanish is a plus

Preferred Experience: Pharmaceutical/Biotech Industry, Hematology, Oncology

Location: Sao Paulo Hybrid (2 to 3 days per week in the office)

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, BeOne SOPs, and local regulations

Essential Functions:

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

• Site Feasibility

  Build knowledge in therapeutic area, local regulations and sites to provide strategic

  recommendations to teams on potential first site(s) to be selected/activated to

  achieve FPI.

• Site Start-Up

  Skilled in driving kick-off and completion of tasks from selection through activation.

  Leverage and build upon existing site partnership data to execute start-up efficiently, reducing cycle times wherever possible.

  Prepare submissions dossiers to Ethics Committees and Regulatory Authorities according to applicable regulations, SOPs and work instructions.

  Review, establish and agree on project planning and project timelines. Ensure overall project efficiency and adherence to project timelines.

• 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 review of essential documents

• Provide Regulatory support after approvals, including submission of core documents to the sites and Regulatory Authority, and Annual/Final reports to Regulatory Authority.

• Complete SSU data entry in CTMS, if applicable

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

• Contribute to the ongoing improvement of SSU infrastructure in the Americas – in the U.S., Canada, and Latin America

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

• Perform the translation process for ethical and regulatory documents

Minimum Requirements – Education and Experience:

Bachelor’s degree or higher 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

Other Experience:

• Knowledge in the execution of clinical trials, understanding of ICH/GCP

• Prioritization of tasks in the achievement of goals

• Strong written and verbal communication skills

• Highly organized

• Diligence in follow through

Supervisory Responsibilities: NA

Travel: Up to 10%

Computer Skills:Intermediate skills in Microsoft Office – Outlook, Word, Excel, PowerPoint, Teams

#LI-Remote

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