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Programme Manager

Job Introduction

We are looking for:
A Programme Manager to manage packages of Metabolism studies and analytical project manage clinical metabolite profiling and identification studies.

At Pharmaron we offer:
  • Vibrant and dynamic employment – we are a highly specialised, growth company operating in a critical sector of the economy – our future is strong and exciting!
  • Opportunities to develop your skills and yourself – our rapid growth brings greater opportunities for you to learn and grow faster!
  • A great team where we all support each other – enjoy your work – after all you spend about a third of your time here!
Key roles and responsibilities:

Study Management
  • Act as Analytical Project Manager on clinical metabolite profiling and identification studies.
  • Prepare analytical work plans, study reports and SOPs as required.
  • Take full responsibility for the conduct of experimental work required to successfully fulfil all the requirements of a study to the timelines stated in the Study Plan.
  • Work closely with clinical site and client to ensure requirements in terms of timelines are understood and can be met.
  • Plan work to ensure revenue recognition milestones on assigned studies are hit in the month, flagging up any issues early. Ensure resource allocated to their studies is effectively utilised.
  • Review data obtained and prepare study updates and study data for discussion internally and for communication to the client/inclusion into reports.
  • Address findings arising from QA audits and process inspections.
      
      
Programme Management
  • Under the guidance of the Team Leader act as a link person between Business Development and Operations at the proposal stage for packages that will require Programme Management support.
  • Liaise with Business Development to raise supplementary proposals for scope changes/additional studies.
  • Under the guidance of the Team Leader manage programmes of studies for a client which extend across different Metabolism areas e.g. ADME, Clinical QRA, Metabolite ID & profiling, In Vitro & DDI and involve external organisations e.g. Clinics and Subcontractors.
  • Work with SDs/the Metabolism Management Team to ensure all necessary pre-study information is obtained from the client and distributed.
  • Work closely with Operations for the scheduling of programmes and making sure they stay on track.
  • Maintain an overview of the “big picture” of assigned programmes of work to ensure client’s overall objectives are being met, while also keeping sight of the detail of the individual projects.
  • Prepare and update Gantt Charts for assigned programmes.
  • Monitor and manage individual project timelines, liaising with clients and with Operations/QA, as required.
  • Under the guidance of the Team Leader discuss any significant changes to agreed timelines with Operations and if necessary escalate to the Director of Metabolism (particularly if they impact dosing or have financial implications).
  • Communicate regularly with clients to ensure their expectations are understood, managed and met as appropriate.
  • Liaise with Chemistry on schedule for synthesis and delivery of radiochemicals for use on managed programmes.
  • Chair and circulate action points from regular telephone conferences with clients and relevant parties as required.
  • Ensure sponsors are kept informed of study progress and there is good communication between different areas of Metabolism and external organisations.
  • Compile regular programme status reports and send to clients.
  • Actively participate in client facility visits where required.
  • Where appropriate advise clients of further available services which could help progress their programme.
  • To study direct other regulated and non-regulated studies as required.
  • Contribute to the review and QC checking of all relevant study data packages and reports prior to submission to Quality Assurance as required.
      
Requirements:
  • Project Management
  • Scientific data interpretation, reporting and presentation skills
  • Effective written and verbal communication skills, including the ability to effectively present scientific findings to colleagues and clients
  • Proficiency in analytical techniques (HPLC/TLC/LC-MS)  
  • Understanding of the drug/agrochemical development process
Our Company: “We are a dynamic, fast-growing company, with an enviable reputation for leading edge science, offering contract research services to some of the world’s leading pharmaceutical companies, solving what were believed to be unsolvable scientific challenges”.

We believe in our ability to relentlessly push forward the boundaries of scientific excellence, delivering solutions for our clients, always operating ethically and with integrity. We take pride in our professionalism and commitment to always deliver our very best work.

Based in Northamptonshire, our Rushden site is a centre of excellence for Radiolabelled Sciences incorporating both Metabolism (which includes Clinical Metabolism, Pre-clinical ADME, In vitro and DDI services, Large Molecule Metabolism, Environmental Fate, Plant Metabolism and Metabolite Identification) in addition to Chemistry (which includes API and IMP manufacture). We offer our employees a supportive teamwork environment, enabling them to develop and liberate their true potential.

  • We offer a competitive salary and a progressive and comprehensive suite of employee benefits.
  • We offer state of the art working environment in our specialist Rushen site.
  • We offer the opportunity for growth and development and will support funding for relevant training and development programmes.
Why Should You Apply?
  • This is an opportunity for you as a Programme Management professional to make a real impact in a highly scientific and regulated environment, demonstrate leadership, ambition and the desire to grow with the department.
  • Build and shape your career in an environment that sets and commits to the highest standards of Chemistry.
  • To be part of a team who support each other, embrace and solve technical challenges and put excellence at the heart of all that we do.
Pharmaron is a premier R&D service company supporting the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities having established diverse drug R&D service capabilities, ranging from synthetic, medicinal, and analytical chemistry, biology, DMPK, pharmacology, drug safety assessment, radiochemistry and isotopically labelled metabolism, chemical & pharmaceutical development to clinical development.  With operations in China, US and UK staffed by over 19,000 employees, Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan, and China.
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