IQVIA
Associate Medical Director- Oncology ,Sponsor-Dedicated(m/w/x)
Full-timeOn-siteSenior
Frankfurt am Main
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IQIQVIA
Medical Director- Psychiatry(m/w/x)
Frankfurt am Main
Full-timeOn-siteManagement
Nejo AI Summary
Global medical advisory for clinical trials and business development in life sciences. Board certification and 2+ years clinical trials experience required. Work with a global team on accelerating medical treatments.
Requirements
- Medical degree from accredited, internationally recognized medical school
- Specialty board certification
- Minimum 2 years clinical trials experience as investigator or medical/clinical expert in Pharma, CRO, or Biotech industry
- Ability to establish and maintain effective working relationships
- Strong communication, presentation, and interpersonal skills
- Good command of English language (written and spoken)
- Robust and current knowledge of scientific, clinical, regulatory, commercial, and competitive landscape in applicable therapeutic area
- Proven consultation and advice skills on multiple assignments
- Initiative and flexibility
- Periodic regional and international travel
Tasks
- Provide medical and clinical advisory expertise
- Participate in Medical Science involvement
- Serve as medical expert during project delivery
- Provide therapeutic and medical expertise for business development
- Serve as Global or Regional Medical Advisor
- Provide scientific guidance to Project Leaders
- Support investigative sites and project staff for protocol issues
- Review and clarify protocol-related documents
- Train project clinical team on therapeutic areas
- Attend and present at Investigator Meetings
- Review and clarify trial-related Adverse Events
- Review Serious Adverse Events with Pharmacovigilance
- Support Analysis of Similar Events with Pharmacovigilance
- Review adverse event coding
- Review Clinical Study Reports and patient narratives
- Attend Kick-Off, weekly team, and client meetings
- Respond to urgent protocol questions 24/7
- Advise on medically sound delivery strategies
- Develop medically related aspects of client proposals
- Review protocols for scientific and regulatory soundness
- Identify target sites and principal investigators
- Anticipate patient recruitment and standard of care
- Attend and present at bid defense meetings
- Participate in strategic business development activities
- Maintain awareness of industry developments
- Author related publications
Work Experience
- 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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IQIQVIA
Medical Director- Psychiatry(m/w/x)
Frankfurt am Main
Full-timeOn-siteManagement
Nejo AI Summary
Global medical advisory for clinical trials and business development in life sciences. Board certification and 2+ years clinical trials experience required. Work with a global team on accelerating medical treatments.
Requirements
- Medical degree from accredited, internationally recognized medical school
- Specialty board certification
- Minimum 2 years clinical trials experience as investigator or medical/clinical expert in Pharma, CRO, or Biotech industry
- Ability to establish and maintain effective working relationships
- Strong communication, presentation, and interpersonal skills
- Good command of English language (written and spoken)
- Robust and current knowledge of scientific, clinical, regulatory, commercial, and competitive landscape in applicable therapeutic area
- Proven consultation and advice skills on multiple assignments
- Initiative and flexibility
- Periodic regional and international travel
Tasks
- Provide medical and clinical advisory expertise
- Participate in Medical Science involvement
- Serve as medical expert during project delivery
- Provide therapeutic and medical expertise for business development
- Serve as Global or Regional Medical Advisor
- Provide scientific guidance to Project Leaders
- Support investigative sites and project staff for protocol issues
- Review and clarify protocol-related documents
- Train project clinical team on therapeutic areas
- Attend and present at Investigator Meetings
- Review and clarify trial-related Adverse Events
- Review Serious Adverse Events with Pharmacovigilance
- Support Analysis of Similar Events with Pharmacovigilance
- Review adverse event coding
- Review Clinical Study Reports and patient narratives
- Attend Kick-Off, weekly team, and client meetings
- Respond to urgent protocol questions 24/7
- Advise on medically sound delivery strategies
- Develop medically related aspects of client proposals
- Review protocols for scientific and regulatory soundness
- Identify target sites and principal investigators
- Anticipate patient recruitment and standard of care
- Attend and present at bid defense meetings
- Participate in strategic business development activities
- Maintain awareness of industry developments
- Author related publications
Work Experience
- 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
IQVIA
Industry
Healthcare
Description
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Not a perfect match?
- IQVIA
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(Sr.) Medical Science Liaison Rare Disease / Tumour(m/w/x)
Full-time/Part-timeOn-siteSeniorMünchen, Köln, Gießen, Mainz, Frankfurt am Main, Göttingen, Erfurt, Leipzig, Dresden - Cencora
.Manager Scientific Affairs(m/w/x)
Full-timeOn-siteNot specifiedBad Homburg vor der Höhe