Biotechnology Jobs in Manchester

• Manchester
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for clinical trials, ensuring GCP compliance, patient safety and data integrity. Builds relationships with investigators, resolves data queries, mentors junior staff and travels up to 40-60% within the region. Embedded in a sponsor-dedicated functional service partnership model.

Investigator Site Files · Trial Master Files

• Manchester
• Senior

Monitors clinical trial sites across selection, initiation, monitoring and close-out visits in line with GCP, while driving subject recruitment and tracking regulatory submissions, CRF completion and data query resolution. Also trains site staff, maintains TMF/ISF documentation and may support site financial management and start-up activities.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Manchester
• £38,448 – £46,970 pa
• Entry level
• Contract

Lead mass spectrometry-based proteomics within a Wellcome Discovery Award consortium studying microbial competition and Type VI Secretion Systems. Design and run DIA proteomics experiments, maintain timsTOF and LC instrumentation, and apply R-based analysis pipelines, publishing findings as lead or co-author.

timsTOF HT · timsTOF Ultra AIP · Liquid Chromatography +1

• Manchester

Field-based role selling laboratory reagents and custom/bulk chemicals directly to customers and through top-tier distributors across Northern UK. You build territory plans, forecast, maintain CRM, train sales reps, and support trade shows, working with clients in pharma, food and beverage, and environmental testing. Requires a chemistry background and frequent travel.

CRM

• Manchester
• Mid-level

Monitors clinical trial sites through selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines, while driving subject recruitment and tracking regulatory submissions, CRF completion and data queries. Works within a full-service, multi-sponsor site management team, training site staff and maintaining Trial Master File documentation.

• Manchester
• Mid-level

Monitors oncology clinical trial sites through selection, initiation, monitoring and close-out visits, ensuring compliance with GCP and ICH guidelines. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within IQVIA UK's multi-sponsor Site Management team, with travel to sites required.

Trial Master File · Investigator's Site File

• Manchester
• On-site
• Entry level

Perform complex clinical procedures such as ECG, phlebotomy, spirometry, cannulation and cardiac telemetry on trial volunteers, and collect and report data per protocol. Support Phase I-IV studies at a hospital-based research facility, ensuring compliance with GCP and SOPs while orienting volunteers and assisting nursing colleagues.

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