Hiring.Camp

Associate Study Start-up Specialist

BeOne

·

4 days ago

Location
São Paulo, Brazil
Workplace
Hybrid
Type
Full-time
Seniority
Entry
Source
Workday

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.

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

Language Requirement: Fluent English Required

Preferred Experience: Pharmaceutical/Biotech Industry, Hematology, Oncology

Location: Sao Paulo Hybrid

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 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 1 year 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:  N/A

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

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.

Skills

GCPExcelClinical TrialsNegotiation

Similar Jobs

30

Study Start Up Associate

Icon · UK, Reading, United Kingdom · Remote

4 days ago

Study Start Up Associate

Icon · Denmark, Copenhagen · Remote

1 week ago

Study Start-Up Associate

Icon · Bulgaria, Sofia · Onsite

1 week ago

Study Start Up Associate

Icon · Malaysia, Kuala Lumpur · Remote

1 month ago

Study Start Up Associate

Icon · Poland, Warsaw +2 · Onsite

1 month ago

Study Start Up Associate

Icon · Denmark, Copenhagen · Remote

1 month ago

Study Start up Associate

Icon · Brazil, Sao Paulo · Onsite

1 month ago

Study Start Up Associate

Alira Health · Munich, Germany +1 · Hybrid

1 month ago

Study Start Up Associate

Icon · Colombia, Bogota · Onsite

2 months ago

Study Start Up Associate

Icon · Regional Guatemala (PRA) · Remote

2 months ago

Study Start Up Associate

Icon · Canada, Burlington · Remote

2 months ago

Study Start Up Associate II - Medical Device - Arden Hills, MN

Icon · US, Blue Bell (ICON), United States of America · Remote

3 days ago

Study Start Up Associate II - Medical Device - Arden Hills, MN

Icon · US, Blue Bell (ICON), United States of America · Remote

3 days ago

Senior Study Start Up Associate

Icon · Taiwan, Taipei · Onsite

3 days ago

Study Start Up Associate I (Clinical Trial Coordinator)

Icon · Brazil, Sao Paulo · Onsite

4 days ago

Senior Study Start Up Associate

Icon · UK, Reading, United Kingdom · Remote

6 days ago

Study Start Up Associate I/ II

Icon · Taiwan, Taipei · Onsite

1 week ago

Study Start Up Associate I

Icon · UK, Reading, United Kingdom +2 · Remote

1 week ago

Study Start Up Associate I

Icon · Thailand, Bangkok · Remote

1 week ago

Senior Study Start Up Associate

Icon · Greece, Athens · Remote

1 week ago

Senior Study Start Up Associate- Regulatory Affairs

Icon · Korea, Seoul, Korea, Republic of · Remote

2 weeks ago

Study Start-Up Associate II

Icon · US, Blue Bell (ICON), United States of America +1 · Remote

2 weeks ago

Study Start up Associate II

Icon · France, Lyon · Remote

2 weeks ago

Study Start Up Associate II

Icon · Canada, Montreal +1 · Onsite

2 weeks ago

Study Start Up Associate I

Icon · Czech Republic, Prague, Czechia · Remote

3 weeks ago

Study Start Up Associate 1

Icon · Mexico, Mexico City · Remote

1 month ago

Study Start-up Associate II

Icon · Brazil, Sao Paulo · Remote

1 month ago

Senior Study Start Up Associate

Icon · France, Paris · Remote

1 month ago

Study Start Up Associate I

Icon · Hungary, Budapest +5 · Remote

1 month ago

Study Start-up Associate I or II (Remote)

Us Theradex · Princeton, NJ, US +1

1 month ago