Join the Feasibility Department to deliver pre-award and post-award feasibility projects, site identification and enrollment modelling. Responsibilities include feasibility analyses (competitive, epidemiology, recruitment), protocol review, site outreach, presenting findings to BD/clients, and engaging with stakeholders including patient advocacy groups. Requires a Bachelor's in life sciences (or equivalent), minimum 5 years relevant experience, professional-level English; postgraduate degree preferred.

The Senior Feasibility Associate/Feasibility Manager will deliver pre- and post-award feasibility analyses (including recruitment, epidemiology, protocol and site/country assessments), undertake site outreach and identification, support enrollment modelling and collaborate with BD, clients, sites and partners. Requires a life sciences bachelor’s degree, minimum 5 years' relevant experience, professional English, strong data/IT and presentation skills, and knowledge of ICH-GCP. Role may be performed remotely in the listed European countries.

Responsible for conducting feasibility analyses, site and country assessments, site identification and outreach, recruitment and enrollment modelling, and presenting findings to business development and clients. Requires a life sciences bachelor's degree, a minimum of 5 years' related experience, professional-level English, and experience with data platforms and MS Office; ICH-GCP knowledge is expected.

Responsible for delivering feasibility deliverables including pre-award RFP input, protocol and assumptions review, site and country analysis, recruitment/enrollment modelling, site identification and outreach, and presenting feasibility recommendations to BD/clients. Requires a life sciences bachelor's degree and a minimum of 5 years' related experience; English professional proficiency and knowledge of ICH-GCP. Role can be covered remotely in the UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.

Responsible for conducting feasibility analyses (competitive, recruitment, epidemiology, protocol review), site identification and outreach, enrollment modelling, and presenting recommendations to business development and clients. Requires a bachelor’s in life sciences, minimum 5 years' relevant experience, strong data/IT skills, and professional-level English. Knowledge of ICH-GCP and experience with oncology/rare disease trials preferred.

Role responsible for conducting feasibility analyses (pre- and post-award), site and country analysis, protocol review, recruitment and epidemiology analysis, site outreach, and enrollment modelling. Requires a bachelor's in life sciences (or equivalent), minimum 5 years' related experience, professional-level English, strong data/IT skills and familiarity with ICH-GCP. Remote in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.

Role involves reviewing, drafting, negotiating and tracking site Clinical Trial Agreements, vendor and other client contracts; coordinating with Clinical Operations and study teams to meet timelines; maintaining contract files and metrics; and contributing to contracting policies and process improvements. Requires a 4-year degree and at least 5 years' relevant experience in CRO/healthcare contracting.

Responsible for leading client solutions and business development, delivering regulatory outsourcing projects on time and within budget, and mentoring project leaders and teams. Requires a university degree in a scientific/technical discipline, extensive life sciences or consulting experience, proven regulatory affairs project leadership and business development skills, and fluent English.

Parexel is recruiting a Central Laboratory Vendor/Project Manager to support global clinical studies from the UK, Poland or Serbia. The role covers oversight of sample collection/processing/storage/shipping, vendor and CRO coordination, ICF/protocol review for sample sections, tracking and reporting of samples and data, and support through study set-up to close-out. Requires clinical research experience (6–8 years) and central laboratory and oncology experience.