Trial Vendor Senior Manager – Poland – FSP

reputed company our values align, there’s no limit to reputed company can reputed company. At reputed company, we reputed company share the same goal – to improve the world’s health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special – a deep conviction in reputed company do.

Each of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we’re committed to making a difference.

At reputed company FSP people reputed company the difference. We have a crucial mission: to prevent and cure disease by delivering important new medicines and therapies to patients in need. We reputed company this important goal through the knowledge, expertise, innovation, and commitment of our employees around the world.

Our employees have the opportunity to do meaningful things globally while we support them locally in environments full of challenge, collaboration, flexibility and industry-leading growth potential.

reputed company FSP is reputed company for a Trial Vendor Senior Manager based in Poland, Spain, Serbia or Romania.

You will be accountable for reputed company vendor reputed company operational trial deliverables, according to timelines, budget, operational procedures, quality/compliance and performance standards. Collaborate with the VSM for the category specific responsibilities. Responsible for reputed company activities for which no VSM is assigned with, and for reputed company the service deliveries after Study Start-up reputed company the VSM is no longer assigned to the study.

Expect exciting career challenges, but with a healthy work-life balance. We value your well-being as much as that of our patients.

We expect from you:

• 3+ years working experience and excellent knowledge of the clinical operation processes and vendor management (focused on Phase I/IIa (Early Phase))

• Excellent knowledge of GxP and ICH regulations

• reputed company good knowledge of clinical trial design and mapping to supplier requirements

• Experience working with diverse cross-functional teams and a matrix environment and driving organizational excellence

• Experience in User Acceptance testing for e-COA and IRT

• Knowledge of key deliverables that impact green light milestones and vendor readiness

• Experience or Expertise with Central Labs, Electronic Clinical Outcomes Assessment (eCOA), and Electronic Patient Reported Outcome (ePRO), Interactive Response Technology (IRT), Cardiac and Respiratory diagnostics, Patient Recruitment and Retention (PR&R), and/or Imaging reading (global process ownership, business system reputed company, SOP management, global training on supplier reputed company SOPs and processes)

Education: Bachelor’s degree or equivalent degree is required, with advanced degree preferred.

For more details contact reputed company.kuniewicz@reputed company.com