Global Clinical Development Lead
Vor 4 Tagen
We are looking for a Clinical Development Medical Director (CDMD) who is responsible for leading the strategic planning and management of the assigned clinical programs from an end-to-end clinical development perspective. As the CDMD, you will oversee the clinical development of the assigned programs and drive the implementation of the clinical development plan. In addition, you will support a capable organisation that is able to operate in a matrix environment and respond quickly to business needs.
**Your responsibilities include, but are not limited to**:
- Providing clinical leadership and strategic medical inputs for all clinical activities in the assigned project or section of a clinical program.
- Leading the development of clinical sections of trial and program level regulatory documents.
- Driving the implementation of the assigned clinical program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/national medical staff where applicable.
- Supporting the (Senior) Global Program Clinical Head (GPCH) in ensuring the overall molecule safety for the assigned section and may act as a core member of the Safety Management Team (SMT) to support overall safety reporting in collaboration with colleagues for patient safety.
- Supporting the Clinical Development Head (CDH) by providing medical inputs into the review of the Clinical Development Plan (CDP), Integrated Development Plans (IDP), and Clinical Trial Protocols (CTP), and contributing to the development of clinical standards for new disease areas.
**What you bring to the role**:
- An MD or equivalent medical degree is required, as well as advanced knowledge and clinical training in the medical/scientific field; 4 years of clinical practice experience (including residency) and certification or eligibility in oncology or haematology preferred.
- At least 7 years of experience in clinical research or drug development.
- Experience in an academic clinical research or industry environment that includes clinical activities in phases I to IV.
- 2 years of contribution to and success in all aspects of drug development, including clinical research, regulatory affairs, and medical affairs.
- Excellent leadership and project management skills, as well as the ability to work in a cross-functional, matrix environment.
- Excellent communication and interpersonal skills, as well as the ability to effectively collaborate with internal and external stakeholders.
NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Luxembourg, Switzerland, Romania, the US and the Czech Republic and we hold labour leasing licences across Switzerland
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