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Medical Manager

Job in Riyadh, Riyadh Region, Saudi Arabia
Listing for: Ipsen Group
Full Time position
Listed on 2026-02-15
Job specializations:
  • Healthcare
    Healthcare Management, Healthcare Administration
Salary/Wage Range or Industry Benchmark: 150000 - 200000 SAR Yearly SAR 150000.00 200000.00 YEAR
Job Description & How to Apply Below
Cookie Notice Medical Manager page is loaded## Medical Manager locations:
Riyadh time type:
Full time posted on:
Posted Todayjob requisition :
R-20811
*
* Title:

** Medical Manager
** Company:
** Ipsen Pharma (SAS)
** About Ipsen:
** Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas:
Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries.

We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!

For more information, visit us at and follow our latest news on and .
*
* Job Description:

**** The role of the Medical Manager is to:
*** Deploy and adapt Ipsen Medical Affairs strategy throughout the Kingdon, including tactics and execution.
* Manage Scientific Information dissemination and maintaining relationships with key partners.
* Coordinate and manage all scientific supporting documentation related to IPSEN products and therapeutic areas where the company is involved
* To coordinate in collaboration with Group Medical department the local performance of clinical trials
** Business Support
*** Ensure compliant collaboration with HCPs and HCOs through Ipsen systems and SOPs
* To manage and mentor MSLs and conduct their performance appraisal for medical affairs and lead medical organisation to deliver effective teamwork
* Sets medical affairs strategy for the portfolio in cooperation with other departments and aligns the medical strategy with regional strategies and plans
* To deploy medical affairs team members including MSLs
* Ensures execution of medical affairs activities in the country with highest standards of quality and compliance
* Accountable for medical pre-launch, launch, and post-launch preparation and execution
* Leads the medical scientific communication, medical education and medical expert/KOL interactions
* Develops and manages long-term relationship with external stakeholders/KOLs
* Whenever requested, provide expert clinical opinion/information to external and internal customers – ensures medical product training for Ipsen sales force staff
* To support Marketing department in the supervise, review, and approval of promotional materials from medical point of view ensuring that all local legal requirements and other applicable (e.g. Ethical codes) as well as those established by the Ipsen Group are met, ensure highest quality of scientific non-promotional materials prepared by medical department as well
* Integrated cross-functional plans and collaboration with Marketing and Access teams
* Maintaining a “library” of relevant articles, presentations provided by experts to IPSEN
* To participate at brand teams, work and campaigns preparation
* Participate at preparation of Budget and Strategic plan with focus on medical activities and their budget management
** Clinical Trial and Development
*** To facilitate and coordinate the participation of Ipsen in clinical trials developed by IPSEN Group
* To ensure Ipsen provides trial feasibility evaluation to global team via dedicated medical advisor.
* To establish, implement, advise and coordinate local clinical study protocols, reports and publications viz. feasibilities.
* Ensure full support for Pharmacovigilance including compliance with Adverse Event reporting and ensure risk management plan implementation
* Ensures providing support and consulting advisory to local group of clinical monitors
* Assist in resolving country specific issues in clinical trial preparation/execution
* To ensure contact with local HCP regarding international as well as local research projects
** Regulatory and Pharmacovigilance Support
*** To…
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