Drug Development Project Manager
- Midlands (UK)
- Contract
- CAPEX Projects
This vacancy has now expired
Working within the Project Management department, we are looking for someone from a Scientific background to help manage projects within the Drug Development area for a Global Pharmaceutical organisation.
This position will initially be based working remotely from home, but there may be a requirement to go to site in East Midlands at some stage. Applicants must therefore be UK based and willing to go to East Midlands if required.
Hours per week for this role will be 37.5 Monday to Friday.
DUTIES TO INCLUDE:
- To maintain a complete understanding of the project requirements, costs, invoicing and associated revenues and support in reporting numbers out to the wider Network
- To help plan, coordinate and undertake client projects ensuring that projects are delivered to agreed quality standards and meet client specifications within agreed deadlines and budget.
- To generate and manage accrual tracking sheets that forecast and record revenue recognition for each aspect of the project and update as and when the project activities dictate.
- To ensure that demonstrable evidence is documented to justify revenue recognition for each aspect for each study.
- To provide progress reports and project financial updates to the Head of Project Management as and when required.
- To schedule regular internal project update meetings with internal stakeholders to assess project progress and report back to the client(s) as appropriate.
- Ensure that all internal and client project work conducted by the team and the individual is documented to a high a standard. This includes the timely completion of all necessary project administration. Constantly strive to develop and support a culture of Continuous Improvement whereby we seek to improve operations, streamline work processes, decrease turnaround times and improve quality.
THE IDEAL CANDIDATE WILL HAVE THE FOLLOWING SKILLS:
- Experience in a commercial environment.
- Detailed knowledge in one or more of the following areas: formulation development, analytical development, pharmaceutical production, quality control/assurance, or regulatory CMC documentation desirable.
- Strong scientific and technical knowledge in Pharmaceutical Development and Manufacturing is desirable.
- Experience of the overall drug development process is desirable.
- Effective project management skills - ability to develop study work plans against tasks, timeframes, milestones resources and dependencies through discussions with internal stakeholders.
- Effective financial skills – good numeracy required and the ability to generate financial and revenue recognition tracking sheets for studies reflecting the work plan.
If this role is of interest, please apply now.
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta part of QCS Staffing does not sponsor Visa applications.
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We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
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