Start Date
Immediate
Expiry Date
20 Jun, 25
Salary
0.0
Posted On
21 Mar, 25
Experience
0 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Regulations, Regulatory Requirements, English, Strategic Thinking, Pharmaceutical Industry, Research, Business Knowledge, Gxp, Epidemiology, Clinical Research
Industry
Pharmaceuticals
KNOWLEDGE, ABILITIES & EXPERIENCE
Experience:
position is responsible for compliance with the ethical and regulatory requirements by health authorities and Ipsen processes and regulations.
IPSEN is an equal opportunity employer that strictly prohibits unlawful discrimination. We recruit, employ, train, compensate, and promote without regard to an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law
Develop and maintain knowledge
RESPONSIBILITIES
Provide scientific information and support
manner to documented unsolicited requests from external stakeholders regarding clinical information
and data in relation to disease specific questions around the product/therapeutic areas he/she is
responsible for, pre-launch communication, on-label or off-label use or any Ipsen’s research programs.
This in alignment with Ipsen’s guidelines and local laws and industry codes and regulations.
approval in relevant systems.
responsible for across Ipsen marketing, sales, and medical functions.
Develop and maintain knowledge
landscape. Ensure this is communicated to the appropriate Ipsen personnel
strategy, by reactively (and proactively where appropriate) providing them with scientific and clinical
data.
therapeutic areas and to produce congress summaries for dissemination to HCPs.
business priorities.
line with the therapeutic area strategy and Ipsen SOPs.
Provide medical brand support and MSL activities
or support of therapeutic area studies as appropriate, and in line with Ipsen SOPs and International
Guidelines to ensure successful completion of the trials and their publication. Where required, provide
budget control and accountability of these programs.
activities.
position is responsible for compliance with the ethical and regulatory requirements by health authorities and Ipsen processes and regulations.