8 months ago
I've partnered with a leading global organisation who are looking for a Senior Global Project Manager to join their growing team. They currently work with 96% of the leading Pharmaceutical and Medical Device companies to deliver Medical Affairs, HEOR and Market Access expertise across multiple therapeutics areas. This is an opportunity to work for an innovative and cross functional team, where change is encouraged and growth is constant.
This role will contribute to real-world data collection projects for pharmaceutical industry clients, in UK and international settings alongside being the primary client contact and ensuring the clients objectives are met throughout and being the internal point of contact for all Global Project Managers.
Perform as the primary point of contact for the client from project start, project handover has occurred from the Business Development team, through to completion of contracted services.
Manage project staff from partner companies in other countries, or third-party vendors. This will include project specific scoping and contracting with partners and vendors, in liaison with the Associate Director, or Director of Project Management.
To provide support and leadership to international CRA teams throughout projects, with regards protocol, therapeutic area, study procedures and SOP training.
To work with the relevant team members to develop data collection and communication guidelines, ensuring consistency between researchers working on projects and enable an effective data cleaning process.
Identification of knowledge and process gaps, and development/delivery of coaching to improve team performance, in liaison with the Director of GPM or Associate Director.
Identify opportunities for new projects or project extensions and inform the Director of RWE/RWE Consultant of new business opportunities.
Primary responsibility for financial and operational oversight of RWE projects/programs, taking a senior client management role.
Working knowledge of Good Clinical Practice/International Council on Harmonisation (ICH) Guidelines and other applicable regulatory requirements.
Comprehensive knowledge of the regulatory approval process for non-interventional research studies and general oversight of clinical research processes outside of UK.
Strong demonstrable experience as a Clinical Project Manager, with experience of managing a cross-functional team from project contract and start up to final deliverables.
5+ years relevant demonstrable experience in an international setting.
Bachelor's degree or Registered Nurse (RN) in a related field, or equivalent combination of education, training, and experience.