AMS Study Manager: Clinical Mass Spectrometry Lead

Pharmaron; Hoddesdon; Sur place; GBP 55 000 - 75 000; Plein temps

Résumé du poste

Pharmaron Hoddesdon is recruiting a Study Manager to lead Accelerator Mass Spectrometry studies, including mass balance, metabolite profiling and IVPK. You will manage timelines, reports and QA reviews, coordinating with clients and internal teams.

The role requires a PhD/MSc/BSc in chemistry or related field, experience in GxP environments, and a track record in drug discovery or development. Mentoring and continuous improvement duties are included.

Qualifications

• PhD/MSc/BSc in Chemistry, Biochemistry, Physics or related subject.
• Experience managing analytical studies in a GxP setting.
• Experience in drug discovery and/or development projects.
• Managing external collaborations.
• Experience coordinating multiple projects to meet requirements.
• Experience supporting Phase I trials (e.g. hADME/SAD/MAD) is desirable.
• Strong written and verbal communication and presentation skills.
• Flexible mindset with initiative.

Responsabilités

• Act as analytical project manager on AMS studies (mass balance, metabolite profiling, IVPK).
• Prepare work plans, study reports and SOPs as required.
• Understand AMS techniques through hands-on training and apply to studies.
• Lead study conduct to meet timelines in the Study Plan.
• Review data and prepare summaries for reporting.
• Collaborate with AMS teams and Pharmaron stakeholders.

Connaissances

Analytical project management

Communication skills

Problem solving

Initiative

Team leadership

Formation

PhD in Chemistry/Biochemistry/Physics or related

MSc or BSc (Hons) in Chemistry/Biochemistry/Physics or related

Description du poste

Pharmaron Hoddesdon is recruiting a Study Manager to lead Accelerator Mass Spectrometry studies, including mass balance, metabolite profiling and IVPK. You will manage timelines, reports and QA reviews, coordinating with clients and internal teams.

The role requires a PhD/MSc/BSc in chemistry or related field, experience in GxP environments, and a track record in drug discovery or development. Mentoring and continuous improvement duties are included.