Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson.

Johnson & Johnson

(Part time) Medical Advisor Psychiatry

Posted Apr 19, 2022
Job ID: JJJP00010740
Location
Beerse
Hours/week
20 hrs/week
Timeline
8 months
Starts: May 2, 2022
Ends: Dec 31, 2022
Payrate range
Unknown
Application Deadline: May 2, 2022 12:00 AM

Johnson & Johnson Worksense (via Randstad Sourceright) is responsible for finding, engaging and contracting talent for the Johnson & Johnson contingent workforce.

 

 

We are currently recruiting a (Part time) Medical Advisor Psychiatry to join our contingent workforce. You will be working in the Johnson & Johnson Medical Affairs team in Beerse, Belgium. This will be an initial contract opportunity, starting from May 2nd until the end of 2022, with possibility of an extension.

 

Location: Off site position with on site access in Beerse

PART TIME position: 50% (Tuesday afternoon, Wednesday and Friday)

 

 

 

Your Responsibilities:

 

Therapeutic area scientific expert

  • Demonstrates continuously updated knowledge of relevant products, treatment paradigms, clinical activities, studies, and healthcare landscape
  • Translates new data, presented at congresses, to the local impact and dynamics.

 

Data generation activities

  • Be the primary contact person for Global Clinical Operations (GCO) or external service providers to discuss key target centers and contacts for new clinical trials for evidence generation activities
  • Coordinates evaluation & approval processes of customer support requests (educational grants, quality improvement grants, investigator-initiated studies)

 

Data dissemination activities

  • Proactive and reactive communication of non-promotional medical scientific data using
  • Multichannel approaches for external stakeholders in accordance with healthcare compliance guidelines
  • Create, review, discuss, and provide approval of proactive and reactive materials for non- promotional activities
  • Review, discuss, and provide approval for promotional activities in iMR
  • Builds MAF medical education plan and maintains overview, and supports MSL with focus on concept/content and internal processes for approval

 

Medical Affairs Leadership and Accountability

  • Supports MTAL in building MAF strategy and responsible to translate MAF strategy into impactful country-specific tactics through regular alignment with MSL/MA team & MTAL
  • Plan, coordinate and lead Advisory Boards, ensuring timely communication of key medical insights with internal stakeholders
  • Provide content training and effective communication of data, key publications or other important scientific or clinical information across TA, together with the MSL
  • Provide cross-functional scientific and medical guidance to internal partners 
  • Collaborate with Strategic Account Management (SAM) to scientifically establish and deepen strategic alliances across the TA
  • In response to any customer service request, collaborate with Medical Information and EMEA Scientific Knowledge Management (SKM) as appropriate to meet customer needs
  • Main internal business counterparts and stakeholders: brand manager, account & sales manager, patient engagement & advocacy manager, health economics and market access manager, real-world evidence manager, business unit manager
  • Responsible to lead pre- and post-approval access process (CUP, NPP, MNP) in situations where patients cannot be treated with currently available and registered treatment options, and cannot be included in ongoing clinical trials
  • Manage assigned portion of Medical Affairs budget
  • Take on role of Study Responsible Physician/Scientist (SRP/SRS) where applicable for IIS or Company Sponsored MAF studies, including Clinical Study Reports (CSR) as appropriate

 

 

 

Minimum requirements: 

  • Scientific degree: medical doctor, pharmacist or degree in biomedical/scientific sciences
  • Relevant experience within Medical Affairs and/or Clinical R&D in the pharmaceutical industry (preferably as MSL or MA) or equivalent significant experience in academic medicine, ideally within psychiatry
  • Languages: Dutch & English, French: spoken, read and written
  • Strong communication skills & project-based working
  • Ability to connect and build professional working relationships with internal business stakeholders/functions
  • Understanding of scientific research, clinical trial design/conduct and interpretation of medical/scientific data (scientific acumen), and ability to translate this into information to inform strategy as well as into designing medical affairs activities
  • Ability to link medical/scientific information with clinical practice in order to create insights and inform medical affairs/CVT strategy (strategic acumen)
  • Learning agility to quickly build deep understanding and knowledge about the use of Janssen medicines within their approved indication

 

 

 

If you meet our requirements and are interested in hearing more about our (Part time) Medical Advisor Psychiatry role, please do not hesitate to apply through the provided link today and a member of our recruitment team will be in touch!


 

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