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Our company is a global pharma company on a mission to help patients worldwide get faster access to lifesaving, innovative, breakthrough therapies.
We operate on 4 continents in over 25 countries and are growing fast.
If you want to be part of our mission and help save patients by getting them the latest treatments, join us!
Our company seeks a Therapeutic Area Manager for the Neuro Rare Diseases Unit.
This role includes independently managing a Therapeutic Area.
Outline strategic policies for several fields and products and implement the policy.
Prepare a plan for achieving and maintaining goals.
Managing human resources.
Responsible for the budget of the Therapeutic Area, planning and monitoring it.
Working closely with overseas partners, having an in-depth understanding of the field and KOL's.
Mentoring employees for personal and career development.
Responsibilities:
- Responsible for managing the product managers and human resources within the unit.
- Mentoring team members, product managers, and product specialists.
- Career development for employees.
- Approving and monitoring business plans.
- Involved in building cooperation between marketing units.
- Maintaining strong relationships with overseas partners.
- Business meetings with overseas partners, training sessions, conferences, etc.
- Monitoring and following up on the unit's goals.
- Locate new companies/new products.
- Implement company's principles and vision.
- Report all safety data received within the working framework and pass it on to the PV dept.
- Work by company's code of ethics and guidelines set by the compliance and regulatory dept.
- Report to BUM.

We are looking for a Clinical Affairs Manager to implement and oversee all activities related to clinical research and clinical studies in the company.
DiA Imaging Analysis provides AI-powered solutions to make ultrasound image analysis smarter and more accessible.
Its AI-based solutions help ultrasound users acquire the right image and analyze it automatically, allowing them to identify clinical abnormalities that are often difficult to find visually and enabling them to make better decisions based on accurate and objective data.
Your role:
Designing and managing the execution of clinical studies that demonstrate medical product safety and efficacy.
Ensuring that trials are conducted in full compliance to GCP.
Full responsibility on sites initiation, site personnel training and monitoring.
Working closely with the principal investigators and study coordinators.
Working with regulatory, development and marketing teams to create scientific publications, clinical marketing material and clinical background required for regulatory submissions.