Oversight Data Manager
Keyrus Life Science is looking for an Oversight Data Manager who will join a team on client's site to direct and have the responsibility to deliver data management services for a study or a group of studies by leading a team of CRO resources.
As an Oversight Data Manager, you will lead a team of Study Data Managers for preclinical, clinical and epidemiological end-to-end data management activities for their assigned project(s) and acts as a Subject Matter Expert. In this sense, you will be the First point of escalation for the study teams where the Study Data Manager at the CRO is the first point of contact at a study level. You will therefore need to understand, mediate and solve complex issues related to data management deliverables and escalate as required.
Moreover, you will act as an advisor to the Study Lead on the data management strategy from protocol to delivery of the clinical database. In this sense, you will provide input to study design, the clinical protocol, study planning and review of study documents.
Your main responsibility will be the management of the outsourced data activities during the execution phase and ensuring that they are delivered as mutually agreed with the study teams. You will also be responsible for leveraging the learnings (success or failure) after study execution to implement, in their area of responsibility, or propose, improvements for the future.
Last but not least, you will develop and maintain excellent professional relations with the clinical teams and other key stakeholders.
You have a master degree in Engineering, Life Science or Computer sciences and have 5 years of experience in the clinical research domain and data management. You have a proven ability to manage the oversight of end to end outsourced processes. You have a good knowledge of global and clinical trials practices, procedures and data presentation. You have strong management and communication skills. You are a team player, have a strong sense of urgency. Your assertiveness and ability to build impactful relationships will play an important role in exercising this function. Last but not least, you are fluent in English (written and spoken).
What we offer
At Keyrus, thanks to the expertise of our people and external partners, each employee is welcomed with a varied integration program. You will join a dynamic and international environment with enthusiastic and professional colleagues.
We invest considerable time and resources in training our staff (technical and non-technical courses) to continuously support you in your personal and professional growth. On top of this, you will receive a complete salary package including attractive extra-legal benefits (company car, petrol card, meal vouchers, group insurance, hospitalization…) based on your background and experience.
Who we are
Keyrus Life Science is an international Consulting, Contract Research Organisation and Functional Services provider with a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our ‘human’ approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.
At Keyrus Life Science we’re proud of our commitment to delivering services of the highest quality, not only skillfully, efficiently and reliably, but also with sincerity and genuine care for our clients’ projects, priorities and reputation. Thus we maintain and advance our vision and our standards, all the while ensuring that we serve your interests better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services.
Keyrus Belgium Offices:
- Office Park Waterloo - Drève Richelle 161 - 1410 Waterloo
- Nijverheidslaan 3, - Strombeek-Bever