Consultant - Senior Manager Medical Research Operations (m/w/d)

Baar  ‐ Vor Ort
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Beschreibung

Consultant - Senior Manager Medical Research Operations

Duration From April till end of the year initially

Location Baar, Switzerland

Description

The Senior Manager - Medical Research Operations (MRO) provides clinical study management expertise and oversight for the execution of post-drug approval research.

In this role, the successful candidate will act as the operational partner in driving data generation program planning and execution. Working across late-stage development and marketed products, the incumbent will drive operations for Phase 4 studies, patient registries, outcomes research, and real-world evidence programs. Activities include study and program planning and budgeting, contracting, start-up, vendor management, site management, tracking and reporting.

The work is collaborative and is performed in conjunction with medical teams in both the global headquarters and at local affiliates. The initial assignment is expected to be in Multiple Sclerosis disease; other disease areas may be assigned.
The position reports to the Director of MRO Study Management and is part of Global Medical Affairs. Remote work arrangement during the remainder of the COVID pandemic is expected.
  • Drive the overall study management strategy for a specific program
  • Provide operational leadership for the program in close collaboration with other leaders and stakeholders
  • Take responsibility for proposal submissions, budgeting, contracting, study management team formation, and study milestones
  • Communicate with Medical Directors, Medical Research Experts, Medical Science Liaisons, medical managers and external investigators on assessment of scientific relevance and feasibility, and provide feedback for proposal improvement
  • Develop external partnerships in collaboration with Medical Directors and scientific experts
  • Take ownership of vendor service procurement and vendor oversight
  • Liaise with global departments to ensure all current active studies are appropriately tracked and documented in the Medical Affairs Research System
  • Coordinate with internal process, infrastructure, and compliance colleagues to ensure appropriate SOPs related to data generation, analysis, and dissemination are followed


Requirements
  • Bachelor's degree in a relevant discipline required. Master's degree preferred.
  • Minimum of 10 years of clinical research experience with CRO/Sponsor Project Management responsibility
  • Fluent in English
  • Strong Project Management skills including risk assessment and contingency planning
  • Demonstrated ability influence and manage teams
  • High degree of learning agility
  • Combination of critical thinking and operational know-how
  • Demonstrated success in working independently
  • High level of customer orientation awareness and focus
  • Strong preference for experience with late phase and observational clinical research
  • Multi-sclerosis disease research experience preferred
  • Exceptional analytical, problem-solving, and troubleshooting abilities
  • Strong written and verbal communication skills


Sthree Switzerland is acting as an Employment Business in relation to this vacancy.
Start
04/2021
Von
Real Staffing
Eingestellt
17.03.2021
Projekt-ID:
2071001
Vertragsart
Freiberuflich
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