Sr. Clinical Trial Manager

Summary

Our client, a global CRO is growing and looking for the best of the best to join their team. We have been asked to partner with them to provide them with Sr. Clinical Trial Management professionals who can assist in this growth and contribute to the overall success of the organization. Culturally, you will be part of a team of industry professionals all with a common goal, to help bring therapeutic assets to patients to increase quality of life and cure disease.

Duties / Expectations of Role

·Provide operations management and oversight of assigned project(s), in accordance to ICH/GCP and all other applicable regulations

·Point of contact for sponsors and key stakeholders for operational project-specific issues and study deliverables

·Responsible for therapeutic knowledge and expertise for assigned studies

·Cross-functional management of project team members and deliverables

·Responsible for study protocol review, study/project management, SOPs, final study reports, and other relevant study duties

·Develop and implement study management plans

·Risk management

·Vendor oversight

·Oversee site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables

Mandatory Requirements

· Degree: BS – Life Science concentration (Biology, Chemistry, RN, etc…)

· Years of experience: 5 years’ experience within CRO setting

·Phase I-IV experience, Phases II-III preferred

·Strong leadership skills

·Project deliverables and timeline management

· Top two skills

oProject/Study management expertise

oCareer stability and progression

Term & Start

· Permanent

· Start date: ASAP

· Onsite: Cincinnati preferred, Dallas or Denver are other options; For remote, MUST have 5 years minimum experience at CTM/PM at CRO

· Minimal travel ~5%

· Benefits included: Healthcare, PTO, 401K, bonus

· Vaccine required: No

· Interview process: 2 rounds, 2 nd may be panel