My client, a global CRO company based in the midlands is currently recruiting for an Associate Project Manager to join their team. This is a great opportunity which has great career progression opportunities and benefits!
The Associate Project Manager liaises with the company's operational divisions, affiliates and sponsors. This position coordinates (in collaboration with Project Managers) the study setup, maintenance and closure activities for identified protocols and/or study programs.
The Associate Project Manager is responsible for supporting the successful delivery and conduct of projects. This position consults on project management issues, and supports overall function of the Project Management group.
Serves as local study coverage for global studies and point on contact for Clinical teams. Ensures timely completion of study activities and deliverables. Documents communication and actions with sponsors or with investigator sites
Manages existing Batch, Supply only, & "In Conduct" studies. Develops new study set-ups as appropriate in collaboration with Tech Ops group
Serves as designated back-up for PM staff (Centralized) and point of contact coverage for Project Managers when out-of office. Reviews and prepares with Project Managers in advance of coverage
Advises project managers on procedural and budgetary items and the necessity for change due to any subsequent study modifications and/or protocol amendments. Monitors monthly Budget to burn reviews and contract modifications
Supports Project Management group with development and implementation of initial study supply orders to include: Creation of initial supply template, and submission of initial shipment requests to Supply Chain Management group
Monitors completion of shipment requests
Schedules group meetings and teleconferences (internal & external), prepares and distributes agenda, records and distributes minutes as required
Monitors assignments and adjust priorities and work schedule to meet deadlines and provide high quality deliverables. Completes additional tasks needed in support of project, client and departmental objectives
Education and Experience:
Bachelor's degree or equivalent and relevant formal academic/vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (at least 2 years) or equivalent combination of education, training, & experience
Knowledge, Skills and Abilities:
Good computer skills
General knowledge of clinical trial processes and programs
Strong attention to detail and problem solving skills
Ability to effectively conduct oral presentations
Demonstrated experience in identification and resolution of technical problems in a professional environment
Ability to maintain a high degree of confidentiality with clinical teams
Ability to attain, maintain and apply a working knowledge of applicable procedural documents
For more information and to apply for this role please call Zoe on +353 1 2784671 or e-mail email@example.com
Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. Www.thornshaw.com Tel: +353 1 2784671