Job Description
Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where our company has codified its 125-year legacy. Our company success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
This role is primarily accountable for the end to end performance for assigned protocols in a country in compliance and regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and externally.
The CRM could be responsible for a particular study for several countries in a cluster.

EXPERIENCE REQUIREMENTS:

Required:

• Minimum 5-6 years of experience in clinical research of which 3 as monitor.
• At least 2 years of experience in proyect managment.
• Advanced level of english.

EDUCATIONAL REQUIREMENTS:

Required:

• Bachelor degree in Science (or comparable).

TRAVEL REQUIREMENTS:

25%

Main Point of Contact for assigned protocols and link between Country Operations and clinical trial team.

• Responsible for project management of the assigned studies: pro-actively plans, drives and tracks execution and performance of deliverables/timelines/results to meet country commitments from feasibility and site selection, recruitment, execution and close out.
• Reviews Monitoring Visits Reports and escalates performance issues and training needs. - Performs Quality control visits as required
• Leads local study teams to high performance: trains in the protocol other local roles, closely collaborates as protocol expert and coordinates activities across the different local country roles ensuring a strong collaboration
• Responsible for creating and executing a local risk management plan for assigned studies
• Responsible for collaboration with functional outsourcing vendors, investigators, other external partners in assigned studies
• Country POC for programmatically outsourced trials for assigned protocols.
• Serves local business needs as applicable in his/her country(If delegated can sign contracts and manage budgets)
• Collaborates internally with HQ functions and locally with pharmacovigilance and to align on key decisions in his/her studies.
• As a customer-facing role, this position will build business relationships and represent our company with investigators
• Shares protocol-specific information and best practices across countries\clusters