The Director Country Head is accountable for strategic and operational management of clinical research and development activities in mid to large-size country
Job Summary
The Director Country Head is accountable for strategic and operational management of clinical research and development activities in mid to large-size country.
This role is responsible for line management of Functional Managers (FM)/Clinical Research Managers (CRM) and other GCO staff, as required.
Contribute to shaping the environment for clinical trials in the country and develop plans and strategy for team engagement with local investigational sites, regulatory bodies and key stakeholders within the country.
Matching Summary
The Director Country Head is accountable for strategic and operational management of clinical research and development activities in mid to large-size country.
Skills & Requirements
Must-have
strategic and operational management
clinical research and development activities
execution of clinical trials
adherence to timelines and budget
compliance with SOPs, HCC, and local regulations
line management of Functional Managers
Health Authority agencies liaison
functional budget management
ICH-GCP knowledge
drug development knowledge
Nice-to-have
foster a culture of continuous improvement
model Credo based culture
shape the environment for clinical trials
visionary leader
transforming organizations
Key Requirements
Bachelor's degree or equivalent required, preferably in Life Sciences
Minimum of 10 years of clinical research experience
Excellent communication and leadership skills
Proven ability to foster team productivity and cohesiveness
Ability to manage complexity under pressure
Proven track record of people and project management
Strong in hiring, training, developing and evaluation of leaders and people managers
Strong decision-making and financial management skills
Flexibility to work in a rapidly changing environment
Effective issue resolution and ability to generate and implement contingency plans
Excellent knowledge of drug development, clinical research operations and regulatory requirements
Proficiency in English
Computer literacy
Strong interpersonal and negotiating skills
Excellent organizational skills
Ability to collaborate and handle multiple priorities within a matrix environment