Live opening · Posted 23 hours ago

CRA Line Manager

Ergomed · Madrid, , Spain
Smartrecruiters Yes Full-time
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At a glance

The key details from the original listing.

Posted 23 hours ago
CompanyErgomed
LocationMadrid, , Spain
Job typeFull-time
Work modeYes
SourceSmartrecruiters
ListedPosted 23 hours ago

About the role

Description supplied by the original job listing.

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.
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

Employment type
Full-time

Work arrangement
Yes

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