- MAC - FULL TIME
CLINICAL MONITORING MANAGER
Closing date for applications: 27 March 2023
MAC is a full-service global Contract Research Organisation (CRO). We also own a network of research sites. Our mission is to serve with honesty and integrity to make an outstanding contribution to human health.
We are seeking to appoint a Clinical Monitoring Manager to join our dedicated Clinical Operations team. This role will be remotely based with travel to sites as required.
FOCUS OF THE JOB:
Responsible for the operational delivery and quality of Clinical Monitoring department.
Contribute to strategy for new business development and provide strategic input on monitoring proposals.
Manage and oversee the delivery of ongoing monitoring programs by supporting multidisciplinary teams
Create fit-for-purpose evaluation designs
Manage partnerships and engagements with clients and partners in the field of CRO.
Ensure effective management of budgets and on-time delivery of project deliverables for monitoring services.
Proactively contribute to organisation development and capacity building activities such as process development/improvement and training.
Contribute to the development of innovative CRO services and support the scale-up of available Global MAC Services.
Work collaboratively with team members, sub-contractors, and clients across multiple countries and time zones.
Facilitate knowledge-sharing and learning, communicating regularly on results and activities in assigned projects and building evidence on common themes across projects.
KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:
A Bachelor's degree or equivalent in a health care or other scientific discipline or equivalent experience.
Familiarity with evaluation theories, tools, and techniques.
Hands-on skill and knowledge on the use of qualitative data for evaluations.
Minimum of 8 years of work experience within the clinical monitoring sector,
Excellent computer skills including use of Microsoft Office.
Excellent oral and written communicative skills. Fluent in oral and written English
Excellent time management skills to organise and prioritise workload.
Able to work independently and proactively.
Excellent inter-personal skills.
Ability to lead by example on process development, departmental and project objectives, and overall business strategy and initiatives.
Ability to work in a collaborative team environment.
Able to proactively identify risks and issues and be able to devise mitigation and contingency plans and solve problems as they arise. Encourage other team members to apply the same approach to seek solutions.
Knowledge of drug development process including the relationship between the CRO industry and pharmaceutical companies.
Knowledge of the regulatory framework that surrounds drug development and the clinical trial process.
Knowledge of clinical trial process; including the interaction between the DM team and clinical operations
Experience in an international setting
Competitive salary in keeping with pharmaceutical industry standards and will reflect experience
Free onsite parking
25 days annual leave (increasing in increments to 30 days after 6 years service)
Your birthday off work
MAC Clinical Research invites applications from highly motivated candidates, with a desire to fulfil their full potential. You will be working with an organisation that sees you as an investment and is keen for you to achieve your career aspirations.
Salary: Competitive + Negotiable £ Apply Now