Clinical Lead III
Premier Research
Remote, Czech Republic
What You'll Be Doing:
- Acts as a leader driving global study and/or program clinical team and departmental engagement, maximizes the efficiencies of the clinical team across studies/program
- Oversight of clinical team tracking and analysis of open action items, protocol deviations and communication reports
- Completes/contributes to the review of the protocol/study design, informed consent forms, case report forms, and other study documents/plans, or delegates to the assigned CL
- Applies a risk-based quality management mindset, contributes to the risk management plan, and supports set up of adaptive risk monitoring system with the study team as applicable
- Works with all functional leads and sponsor to identify data related issues and risks to clinical activities; assists CLs in the development of mitigation plans to minimize risk
- Supports the PM, regional CLs, and/or appropriate line managers to ensure team members are adequately resourced to the project for the entire duration of the study
- Oversight of financial health of clinical activities including support with identifying out-of-scope tasks from the Premier clinical team and ensures pre-approval of these tasks by the PM and Sponsor, as required
What We Are Searching For:
- Bachelor’s degree, or its international equivalent from an accredited institution, in a clinical, biological, scientific, or health-related field; or equivalent work experience
- 9 years of clinical research experience as a CRA, CL or PM of which at least 4 years of clinical monitoring (or related) experience is required
- 3 or more years of previous Clinical Oversight experience or equivalent)
- Provided guidance, mentoring and training for Clinical Leads on a global study and/or program clinical program
- Supported clinical staff as a Subject Matter Expert for processes, systems, or tools
- Expert presentation skills, including bid defense experience
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