Descripción del empleo
Join us on our exciting journey!
IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
IQVIA™ Real-World Evidence Solutions (RWES) is a fast-growing and highly successful business, focusing upon delivering tangible business results to our clients across healthcare value chain who are the decision-makers and business managers across the international pharmaceutical and healthcare industries. You will join an innovative team of c.20+ individuals with a high seniority level leading global offering development, strategy & capability build, and large scale client engagements.
RWES central develops strategic business cases for investment in acquisitions/organic business growth
Creates strategic thought leadership
Supports complex business development options taking a leadership role around RWE
Runs complex new engagement types with clients – supporting to get most value of high cost investments in RWE data, assets and capabilities
With direct access to the world's most comprehensive information, analytic and consulting/research resources, and healthcare intelligence tools, RWES experts deliver deep insights into pathway design, effectiveness of healthcare interventions and products, and value for money. We are one of only a few organizations that integrate real-world evidence (RWE), health economics, outcomes research, consulting, and health intelligence tools at the national and international level across the healthcare value chain.
As part of the Observational team this role is to coordinate and project manage national and international clinical study fieldwork of multiple and multi-country projects
Coordinate and project manage study fieldwork of multiple, multi-country projects within client deadlines.
Set guidelines and write study protocols.
Supervise teams, help new employees integrate.
Monitors study logistics.
Detect possible deviations or problems in study fieldwork and find best solution.
Manage Ethical Committee submission within Control and Quality Assurance.
Reporting project development directly to clients
Review the monitoring plan and monitoring report.
Participate in customers and investigators meetings.
Administration control of the fees and expenses during the Project (travels, meetings, investigators payment).
Work within Quality Assurance SOP's; follow up SOP's, attend training, participate in internal and external audits, support SOP's update to Quality Assurance
Support proposal development
Experience and skills
At least 2 relevant years experience working in clinical observational studies
Experience of working in sizable/multi-disciplined teams and supervising staff
Must be organized with strong capability in managing projects and juggling priorities so that deadlines are met while retaining consistently high quality outcomes
Experience of developing credible relationships (remotely) with senior level managers and executives
Excellent communication, written and verbal with strong client influencing skills
Ability to liaise comfortably with regulatory authorities, investigators and other study groups
Demonstrable analytical, interpretative and problem-solving skills
Flexible approach, prepared to adapt and reprioritize to meet clients and internal needs
Basic knowledge of Microsoft Office, particularly Excel and Powerpoint
Must be fluent in English, written and verbal
Life sciences degree
Nice to have: monitor of clinical trials.
We know that meaningful results require not only the right approach but also the right people
. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.
Whatever your career goals, we are here to ensure you get there!
We invite you to join IQVIA™.
- Carnet de conducir
- Carta de motivación