Description
The Associate Clinical Research Manager (aCRM) is responsible for overseeing local operational clinical trial activities, ensuring compliance with regulations and guidelines, and building relationships with investigators and external partners.
Job Summary: The aCRM will have a significant impact on the delivery of country-specific trial commitments and objectives, and will be responsible for making decisions independently and overseeing important activities relevant to clinical research activities in the country.
Responsibilities:
- PERFORMANCE: Accountable for performance and compliance for assigned protocols in a country (30%)
- MANAGEMENT: Pro-actively drives execution and performance of deliverables/timelines/results to meet country commitments (20%)
- QUALITY OVERSIGHT: Responsible for quality and compliance in assigned protocols in country (20%)
- EXTERNAL CUSTOMER FACING: Responsible for collaboration with functional outsourcing vendors, investigators, and other external partners (20%)
- INTERNAL COLLABORATION and STRATEGY: Collaborates internally with local PV, Regulatory, GMA/GHH to align on key decisions in countries (10%)
Requirements:
- University/college degree (life science preferred), or certification in a related allied health profession
- Minimum of six-eight (6-8) years of clinical research experience
- Thorough knowledge of ICH Guidelines and GCP
- Fluent in local office language and in English, both written and verbal
- Good organizational and time management skills
- Excellent communication skills, oral and written