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&#**Apply on the
website**;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.
*Responsibilities:*
? 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
*Job Qualifications*
*Education and Experience:*
? Bachelor&#**Apply on the website**;s degree or equivalent and
relevant formal academic/vocational qualification
? Previous experience that provides the knowledge, skills, and
abilities to perform the job (comparable to 0 to 2 years&#**Apply on
the website**;) 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 ?a working knowledge of applicable
procedural documents
For more information and to apply for this role please call *Zoe on 1
or e-mail *
Thornshaw Scientific Recruitment is a leading Irish provider of
specialist Scientific Recruitment. Part of the CPL Group. Tel: 1 Location: Not Specified
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&#**Apply on the
website**;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.
*Responsibilities:*
? 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
*Job Qualifications*
*Education and Experience:*
? Bachelor&#**Apply on the website**;s degree or equivalent and
relevant formal academic/vocational qualification
? Previous experience that provides the knowledge, skills, and
abilities to perform the job (comparable to 0 to 2 years&#**Apply on
the website**;) 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 ?a working knowledge of applicable
procedural documents
For more information and to apply for this role please call *Zoe on 1
or e-mail *
Thornshaw Scientific Recruitment is a leading Irish provider of
specialist Scientific Recruitment. Part of the CPL Group. Tel: 1
We need : English (Good)
Type: Permanent
Payment:
Category: Others
