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Clinical Research MD - Belgium   we are looking for a Clinical Research MD

BrightOwl managed [?] Project on hold

Functional titles : Clinical Research Physician
Project Types : Permanent position ,
FTE : 100 %
Min.Experience : 3 year
Start Date : ASAP
End Date : N/A
Posted on : 21 June 2017

Project is currently here

Step 1
Application
Step 2
BrightOwl Screening
Step 3
BrightOwl Interview
Step 4
Company Screening
Step 5
Company Interview
Step 6
Budgets & Contracts
Step 7
Position filled

Project Description

ESSENTIAL FUNCTIONS: 

  • Lead the project scientists, ensuring appropriate training, mentoring, and supervision across the assigned study/studies within the clinical development program
  • Work closely with functional partners (Data Management, Biostatistics, Regulatory, GCO, QMMC, GMS) to ensure an integrated and strategic approach to flawless execution and systematic oversight of study protocol(s) in late development in close collaboration with key functional stakeholders
  • Provide support for clinical study/studies within a development program including:
    • Working closely with the colleague study responsible physicians and clinical project scientists in collaboration with GCO and GMS to ensure comprehensive medical monitoring, thorough and timely responses to address site issues and eligibility questions, and detailed, real time review of serious adverse events and deaths
    • Working in partnership with colleague study responsible physicians and clinical project scientists to ensure development of high quality study protocols including use of consistent processes/standards across studies
    • Collaborate with the Clinical Leader, Clinical Project Scientists and Procurement on key study design elements including assessment of complexity and cost of protocol-required evaluations
    • Participate in strategic study start-up planning in collaboration with GCO, C&G, and RTAEs including early site assessment, feasibility, and use of simplified contract and budget templates to accelerate rate of site activations
    • Co-lead and oversee clinical development/authorship of informed consent forms, eCRFs, study manuals, clinical study reports, and regulatory submission documents 
    • Work closely with Medical Writing to support protocol or protocol amendment completion
    • Work closely with Clinical Leader, Project Physician, Regulatory and GCO to address protocol questions from Health Authorities and Ethics Committees in a consistent fashion
    • Work closely with GCO to track study recruitment, and implement action plans to address early impediments to study enrollment 
    • Work closely with Quality Management & Quality Assurance to review audit findings and implement effective corrective action plans
    • Work closely with clinical scientists and data management to support medical review and data query resolution
    • Interact with clinical investigators and Key Opinion Leaders as appropriate
    • Work with GCO to provide oversight of CRO/study vendors’ performance as it relates to study start-up and conduct 
    • Work with the Clinical Leader, with Data Management and with Statistics on analysis of study results and completion of study reports
  • Work with the Clinical Leader to support the development and compilation of NDA/MAAs and to support responses to Health Agency questions and HA presentations post-filing
  • May review/co-author medical publications emerging from clinical trial results

This is not an exhaustive, comprehensive listing of job functions. May perform other duties as assigned.

 

PRINCIPAL RELATIONSHIPS:

Contacts Inside the Company: 

  • Members of the Clinical and Compound Development Teams
  • Therapeutic Area VPs of Clinical Research

Contacts Outside the Company: 

  • May act as a liaison between company and clinical investigators, vendor managers, and CROs
  • May be asked to assess and plan for external clinical research opportunities in collaboration with Clinical Leader and BD
  • May interact with medical consultants  in concert with senior clinical staff,  in conducting IDMC and Investigator meetings as well as Advisory Boards

Supervision: 

  • Reports to the Clinical Leader of a late stage development program
  • Leads the clinical project scientist members of study team(s), providing effective direction, supervision, and mentoring

Others

Project FTE 100%
Work from home:   Not Allowed
International Travel:   Yes
No. of Positions:   1

Personality

Adaptability Analytical thinking Approachability Assertiveness Collaboration Creative thinking Efficiency Flexibility Independence Organization Optimism Problem solving Responsibility Sociability Trust

Knowledge

Clinical trials Clinical research oncology Urology LCD English Good Clinical Practice (GCP) Regulatory Requirements oncology clinical trials protocol development

Skills and Expertise

protocol development medical review oversight of study data quality and safety

Degree

Ph.D. MD

Languages

English
Full Proficiency
Mandatory

Desired Skills & Experience

Required Technical Knowledge and Skills:

  • Fluent in written and spoken English with excellent communication skills
  • Working knowledge of the use of Microsoft suite of software products including Excel and Word
  • Knowledge of Good Clinical Practices and regulatory requirements for the conduct of high quality oncology clinical trials
  • Experience in protocol development, medical review, oversight of study conduct, data quality and safety is considered a plus.

What we offer

What’s in it for you…?

“Caring for the world, one person at a time…”

As an employee we consider you as our most valuable asset.  We take your career seriously. 

As part of a global team in an innovative environment your development is key and our day-to-day responsibility.