Director of Clinical Projects, Clinical Assessment Technologies
New
United KingdomFull-TimeDirector
Salary not disclosed
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Job Details
- Experience
- 10 years clinical trial experience
- Required Skills
- GCPMS Office
Requirements
- Master’s Degree in life sciences or equivalent.
- At least 10 years clinical trial experience with clinical assessments.
- Experience independently organizing and conducting projects and presenting at Investigators’ Meetings.
- Preferred 4+ years of experience managing team members or providing direct clinical mentorship.
- Strong applied knowledge of pivotal efficacy measure administration conventions.
- Knowledge of operational aspects of Phase I-IV clinical research trials.
- Experience working with a Contract Research Organization or Rater Training Organization.
- Excellent knowledge of SOPs, ICH, GCP, and regulatory guidelines.
- Strong proficiency in MS-Office (Word, Excel, Teams, PowerPoint).
- Strong organizational, detail-oriented, and communication skills.
- Willingness to travel.
Responsibilities
- Engage with senior management to establish strategic department initiatives and objectives.
- Drive new QMD developments, including authoring and reviewing QMD documents and guidance documents.
- Participate in the identification, development, and improvement of service arms.
- Drive business development activities, including inputting into proposals and participating in capabilities and bid defense activities.
- Identify clinical needs for projects and review them with clinical staff and leadership.
- Accountable for the development of assessment training content and plans ensuring compliance with protocol, copyright, and sponsor requirements.
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