top of page

Medical Lead - MD (Doctor of Medicine)

TYPE

Full Time / CDI

REFERENCE

509664

LOCATION

Paris - Hybride

Description

I'm a paragraph. Click here to add your own text and edit me. It’s easy. Just click “Edit Text” or double click me to add your own content and make changes to the font. Feel free to drag and drop me anywhere you like on your page. I’m a great place for you to tell a story and let your users know a little more about you.

This is a great space to write a long text about your company and your services. You can use this space to go into a little more detail about your company. Talk about your team and what services you provide. Tell your visitors the story of how you came up with the idea for your business and what makes you different from your competitors. Make your company stand out and show your visitors who you are.

What you will do

I'm a paragraph. Click here to add your own text and edit me. It’s easy. Just click “Edit Text” or double click me to add your own content and make changes to the font. Feel free to drag and drop me anywhere you like on your page. I’m a great place for you to tell a story and let your users know a little more about you.

This is a great space to write a long text about your company and your services. You can use this space to go into a little more detail about your company. Talk about your team and what services you provide. Tell your visitors the story of how you came up with the idea for your business and what makes you different from your competitors. Make your company stand out and show your visitors who you are.

Who you are

I'm a paragraph. Click here to add your own text and edit me. It’s easy. Just click “Edit Text” or double click me to add your own content and make changes to the font. Feel free to drag and drop me anywhere you like on your page. I’m a great place for you to tell a story and let your users know a little more about you.

This is a great space to write a long text about your company and your services. You can use this space to go into a little more detail about your company. Talk about your team and what services you provide. Tell your visitors the story of how you came up with the idea for your business and what makes you different from your competitors. Make your company stand out and show your visitors who you are.

What they offer

I'm a paragraph. Click here to add your own text and edit me. It’s easy. Just click “Edit Text” or double click me to add your own content and make changes to the font. Feel free to drag and drop me anywhere you like on your page. I’m a great place for you to tell a story and let your users know a little more about you.

This is a great space to write a long text about your company and your services. You can use this space to go into a little more detail about your company. Talk about your team and what services you provide. Tell your visitors the story of how you came up with the idea for your business and what makes you different from your competitors. Make your company stand out and show your visitors who you are.

Got what it takes?

About the job

You will be joining a French Pharmaceutical company based in Paris. The company is well established in the market for decades having mature products already on the market as well as its own research centre. They are investing in development of new innovative product targeting disease with unmet medical needs.

You will be leading and driving the clinical development strategy for the programs you will be in charge, as well as having your hands-on on key activities. Working closely with the Clinical Operation team, Regulatory team and external partners such as the CRO. You will have the full overview on the program you will be leading and able to make a difference.

Your missions

• Build and manage the clinical strategy for the clinical programs that are assign to you.
• Responsible for the medical activities such as: design of the protocol, synopsis, data collection and final reports.
• Collaborating with internal and external team such as: Pre-clinical, Regulatory Affairs, Clinical operations, CROs…
• Participation and management of the CROs
• Perform Medical Monitoring.

Your Experience

• You have a Medical Degree (Medical Doctor) with an experience in Neurology
• 3/5 years of experience in the Pharmaceutical industry OR Biotech.
• Minimum of 3 years of experience in the clinical research with CNS products working with the clinical Trial Protocol, Clinical development plans…
• Speaking English & French is a nice bonus to have.

bottom of page