CRA Line Manager

• Serve as main point of contact for CRAs for any non-project specific needs. 
• Manage performance and support training needs and growth opportunities of CRAs. 
• Communicate regularly with CRAs to ensure their knowledge understanding and compliance with assigned project goals and departmental and corporate strategies and objectives. 
• Plans and implements resource solutions for new and ongoing projects working in collaboration with Resourcing team. 
• Support to determine and operationalize corporate strategy and vision for continued organizational growth. 
• Participate in activities related to CRA recruiting interviewing and hiring. 
• Conduct new employee orientation and onboarding. 
• Participate in project related meetings with other members of Clinical Operations leadership where needed. 
• Ensure ongoing evaluation of CRA performance including oversight of and performance of monitoring evaluation visits. 
• Assist in the development of department quality standards and programs. 
• Assist in Clinical Operations SOP/WI development/review processes. 
• Establish & support strong professional relationships with internal and external stakeholders by building trust open communication and managing day-to day operational issues. 
• Review and approve timesheets and discuss CRA utilization during regular calls. 
• Perform regular monthly calls with all direct reports to assess workload balance performance upcoming deliverables priorities compliance to expected tasks. 
• Review and approve non-billable expenses. 
• Initiate and oversee Performance Improvement Plan with CRAs as required.

Qualifications :

• BA/BS in a Life Science field or commensurate experience

EXPERIENCE

• Demonstrated experience in clinical research. 
• Prior site monitoring experience including experience managing CRAs

SPECIAL SKILLS

• In-depth knowledge and experience of the drug development process including study initiation clinical monitoring drug safety regulatory affairs data management and analysis and clinical study report generation. 
• Ability to travel approximately 20% both domestically and internationally. 

LANGUAGE SKILLS

• Fluent in English

Additional Information :

When you join Ergomed Group you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. Youll join a passionate and collaborative team of experts in clinical research pharmacovigilance and quality consulting.  

We are diverse in many ways yet our values unite us. Our values are how we work not words on a wall. If they sound like you you will feel at home here. 

• Quality: we hold ourselves to the standard patients deserve. 

• Integrity and trust: we do the right thing especially when it is hard. 

• Drive and passion: we care about the outcome because someone is waiting on it. 

• Agility and responsiveness: we move quickly because patients cannot wait. 

• Belonging: everyone is welcome and every voice counts. 

• Collaborative partnerships: we go further by going together. 

We look forward to welcoming your application. 

Remote Work :

Yes

Employment Type :

Full-time