Senior Clinical Project Manager - Cro

Position:  Senior Clinical Project Manager - Small CRO
​Senior CPM / Family-owned CRO / International Studies /
Location:
Remote or Hybrid / Job Type: Permanent /
Schedule:
Full Time / Salary: up to 70,000 (depending on experience)
RBW Consulting are delighted to announce an exciting opportunity on behalf of one of our close clients. This company is a family owned European, full-service Contract Research Organization. They have been supporting clients with international studies for over 25+ years and value their employees highly. To ensure their staff are happy they have created a friendly and flexible environment where all staff are able to develop their skillset and talents.
Through continuous training and access to resources, employees here consistently improve their knowledge and professional development. All of this has led to below industry average for turnover rates internally.
Due to recent funding from their parent company, this CRO are expanding their clinical operations team in Europe. They are winning new business regularly meaning more staff are required to cater to their clients needs. Here you will work with interesting sponsors within respiratory, ophthalmology, oncology, rare disease, or medical device studies, where they have a plethora of expertise.
This is a great opportunity to join a small CRO that is rising through the ranks to become a major competitor within the global CRO industry.
Key Responsibilities Initiates and manages all operational study/project activities and serves as primary point of contact for the assigned Core Project teams
Translates protocol/project strategies from a concept into an executable study/project
Focuses upon the operational integrity and feasibility of individual studies utilizing a variety of resource solutions to ensure the most effective, efficient, and high quality study/project is designed and executed
Participates in and influences the operational strategy for study/project delivery including milestone deliverables to optimize use of time, cost and resources
Participates in the identification, assessment and mitigation of risks at the study level
Maintains continuous communication between partner lines, strategic partners, Clinical Research Units (CRU), contractors and vendors
Optimize Operational Control and Effectiveness Assures close partnership with study investigators to assure successful study delivery and high quality data Fosters positive community attitudes and volunteer trust through professional behaviour and ongoing communication
Skills, Knowledge and Experience Life science-related degree or equivalent
Proven experience in project/study management as well as a background in monitoring
Matrix Leadership experience
Proficient using Office applications (PowerPoint, Excel, Word, Outlook, etc.,)Outstanding organizational capacity for smooth exchanges with Core Study Teams, PIs, Regulatory, and Clinical staff
Benefits
Competitive Salary Great insurance coverage (group and hospitalization)
Meal vouchers
Internet allowance
Company Car & fuel allowance (situation dependent)
Regular face-to-face or telephone meetings with your Dedicated Line Manager Full annual performance review process
Ad-hoc team events and end of year party
Career opportunities within Full Service and Single Sponsor teams both locally and internationally
Employee satisfaction survey - your feedback is important for continuous improvement
To apply :
We are an equal opportunities Recruitment Business and Agency Discipline(s):
Clinical Research, Clinical Operations, CRO & Vendor Services Job type:
Permanent