Key Responsibilities
* Lead cross-functional teams responsible for clinical study delivery and serve as primary point of contact for leadership and oversight.
* Provide operational input into protocol development and oversee the creation of study-specific documentation.
* Ensure compliance with clinical trial registry requirements and identify outsourcing needs for studies.
* Manage risk assessment and mitigation strategies at the study level and lead feasibility assessments to select relevant regions and countries.
Requirements
To be successful in this role, you will need to have exceptional interpersonal and leadership skills, apply advanced expertise to implement strategic direction, and demonstrate expert knowledge in planning, executing, and problem-solving.
You should also have strong budget management experience, be able to build and lead productive study teams, and apply advanced negotiation and interpersonal skills to vendor management.
In addition, you should have extensive experience in global clinical trial operations, knowledge of ICH/GCP and regulatory guidelines, and advanced project management skills.