27 Biopharmaceutical Leadership jobs in Reading.

Hiring now: Clinical Data Mgr Homebas @ Iqvia, Clinical Research Associa @ Intuitive , Cra Ii @ Psicro, Associate Dirdir Of Biost @ Recursion, Graduate Medical Affairs @ Biogen, Sr Site Mgr @ Johnson Jo, Clinical Scientist Fellow @ Boston Sci, Exec Dir Pv Strategy @ Ergomed, Sr Proposal Writer @ Syneos Hea, Sr Technical Expert Sr To @ Syngenta.Explore more at jobswithgpt.com.

🔥 Skills

clinical trials (5) Oncology (4) project management (4) process improvement (4) compliance (3) training (3) Regulatory Compliance (3) biostatistics (3) regulatory submissions (3) pharmacovigilance (3)

đź“Ť Locations

Reading (5) Oxford (4) Maidenhead (4) High Wycombe (4) Farnborough (3) Guildford (2) Bracknell (2) Abingdon (2) Hemel Hempstead (1)
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Iqvia

Clinical Data Manager - homebased (FSP) Reading
Skills & Focus: Clinical Data Manager, data management, clinical data review, Oncology, Cardiovascular, therapeutic area, eCRF, regulatory guidelines, CDM deliverables, leadership
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 4 years Data management experience
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Project Specialist - Clinical Registry Coordinator Reading
Skills & Focus: clinical registry support, clinical trials, data integration, project management, vendor management, timely delivery, compliance, document submission, disclosure planning, healthcare intelligence
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: A minimum of 3 years of relevant pharmaceutical/scientific experience in a clinical development environment.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Dedicated Line Manager, sponsor-dedicated Reading
Skills & Focus: clinical staff, clinical studies, resource allocation, project management, leadership skills, performance evaluation, employee relations, regulatory requirements, training, quality control
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Prior Line Management and Project management experience of at least 3 years is essential.
Type: Full-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Intuitive Surgical

Clinical Research Associate Reading
Skills & Focus: Clinical Research, Monitoring, Regulatory Compliance, Data Integrity, Clinical Trials, Pre-market Studies, Post-market Studies, Clinical Affairs, ISO-14155, Good Clinical Practices
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 3 years in medical device industry in Clinical Affairs/research function with evidence of full monitoring responsibilities.

Psicro

CRA II Oxford
Skills & Focus: clinical research, monitoring visits, study startup, CRF reviews, source document verification, site communication, study activities, compliance monitoring, regulatory approval, data quality

Recursion

Associate Director/Director of Biostatistics Oxford
Skills & Focus: biostatistics, clinical trials, statistical analysis, Oncology, regulatory submissions, data standards, programming in R, project management, trial design, GCP, ICH, CDISC
About the Company: Recursion is a clinical stage TechBio company leading the space by decoding biology to industrialize drug discovery. Enabling its mission is the Recursion OS, …
Experience: 8+ years of biostatistics experience in a pharmaceutical or biotechnology company, including 5+ years of serving as Lead Biostatistician across multiple therapeutic areas (Oncology preferred)
Salary: $168,000 - $242,000 USD
Type: Full-time
Benefits: Eligible for bonuses and equity compensation + comprehensive benefits package for United States based candidates.
Associate Director/Director of Biostatistics Oxford
Skills & Focus: biostatistics, Oncology, clinical trials, statistical analysis, trial design, regulatory submissions, statistical workflows, programming, GCP, CDISC
About the Company: Recursion is a clinical stage TechBio company leading the space by decoding biology to industrialize drug discovery. Enabling its mission is the Recursion OS, …
Experience: 8+ years of biostatistics experience in a pharmaceutical or biotechnology company, including 5+ years as Lead Biostatistician
Salary: 168,000 - 206,000 USD / 212,000 - 258,000 CAD / 89,000 - 109,000 GBP (Associate Director); 198,000 - 242,000 USD / 250,000 - 305,000 CAD / 104,000 - 127,000 GBP (Director)
Type: Hybrid
Benefits: Annual bonus, equity compensation, comprehensive benefits package.
Physician, Clinical Development Oxford
Skills & Focus: clinical trials, drug development, AI/ML integration, patient recruitment, medical governance, clinical oversight, regulatory documents, infectious disease, big data, evidence-based strategy
About the Company: Recursion is a clinical stage TechBio company leading the space by decoding biology to industrialize drug discovery. Enabling its mission is the Recursion OS, …
Experience: MD required, with 5+ years’ experience in Clinical Development
Salary: $284,000 - $346,000 (based on experience)
Type: Full-time
Benefits: Bonuses, equity compensation, and comprehensive benefits package

Biogen

Graduate, Medical Affairs UK & Ireland Maidenhead
Skills & Focus: Medical Affairs, Medical Information, regulatory standards, compliance, training materials, scientific slide decks, stakeholder engagement, cross-border activities, continuous learning, process improvement
Type: Hybrid
Senior Manager, Regulatory Affairs UK & Ireland Maidenhead
Skills & Focus: regulatory, affairs, compliance, UK, Ireland, regulatory strategy, pipeline, product portfolio, stakeholders, market access
Experience: Experienced regulatory affairs professional
Type: Hybrid
Aggregate Report Senior Scientist Maidenhead
Skills & Focus: aggregate reports, PSURs, DSURs, PADERs, pharmacovigilance, safety queries, medical safety, scientific safety, process improvement, global safety compliance

Johnson & Johnson

Senior Site Manager High Wycombe
Skills & Focus: Senior Site Manager, Oncology, Clinical Trial Monitoring, Good Clinical Practice, Regulations, Project Manager, Clinical Trial Support, Team Player, Problem Solver, Data Management
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: 2-3 years of clinical trial monitoring experience preferred
Type: Full-time
Benefits: Competitive salary and extensive benefits package. Flexible working environment and career development opportunities.
Head of European Local Operating Company Regulatory Affairs & Regional Regulato… High Wycombe
Skills & Focus: Regulatory Affairs, Innovative Medicine, Leadership, Talent Development, Strategic Alignment, Submissions, Compliance, Business Support, Patient Access, Team Management
About the Company: Johnson & Johnson is a company dedicated to health care innovation, empowering the development of treatments that are smarter and less invasive with a focus on…
Type: Hybrid
Sr, Manager, Trial Delivery Leader, Oncology High Wycombe
Skills & Focus: clinical trial delivery, operational oversight, cross-functional team, budget management, timelines, quality, risk management, Health Authority inspections, process improvement, employee engagement
About the Company: Johnson & Johnson is a global leader in healthcare innovation committed to building a world where complex diseases are prevented, treated, and cured.
Experience: Minimum of 8 years in Pharmaceutical, Healthcare or related industries.
Type: Hybrid

Boston Scientific

Clinical Scientist, Fellow - EMEA Hemel Hempstead
Skills & Focus: clinical trial, study design, data interpretation, regulatory submissions, medical devices, clinical research, scientific evidence, cross-functional collaboration, Good Clinical Practices, biostatistics
About the Company: Boston Scientific is a leader in medical science, committed to innovating medical solutions that improve patient lives.
Experience: Minimum 7 years of experience in clinical research within the medical device industry.
Salary: competitive salary based on market insights
Type: Hybrid
Benefits: Opportunities for professional growth, cross-functional collaboration, and meaningful impact in shaping the future of c…

Ergomed

Executive Director, PV Strategy Guildford
Skills & Focus: pharmacovigilance, regulations, EU/UK QPPV, consultancy, audits, training, regulatory documents, communication skills, leadership, collaboration
Executive Director, PV Strategy Guildford
Skills & Focus: pharmacovigilance, regulations, EU/UK QPPV, PV processes, audits, gap analysis, consultancy services, training, drug safety, client-facing reports

Syneos Health

Senior Proposal Writer Farnborough
Skills & Focus: biopharmaceutical, business development, clinical trials, communication, project management, strategies, qualitative research, quantitative research, technical writing, stakeholder management
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Clinical Trial Specialist Apprentice Farnborough
Skills & Focus: Clinical Trials, Apprentice, Biopharmaceutical, Patient Access, Clinical Operations, Data Management, Pharmacovigilance, Regulatory Affairs, Biometrics, Research
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Minimum 5 GCSEs grades 9 to 4 (A* to C) including Maths and English language. Have/be predicted to achieve 80 UCAS points, ideally including Biology and one other science.
Type: Apprenticeship
Benefits: Competitive annual salary, private healthcare, pension.
Sr Site Contracts Lead Farnborough
Skills & Focus: site contracts, clinical study agreements, negotiations, contractual language, investigator grant budgets, escalation, industry trends, risk mitigation, strategic planning, mentorship
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Strong experience in a CRO/pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience.

Syngenta

Senior Technical Expert – Senior Toxicologist Bracknell
Skills & Focus: mammalian toxicology, toxicology studies, regulatory requirements, technical strategies, stakeholder management, technical leadership, innovative strategies, training development, science-led, product safety
About the Company: A global leader in agricultural science involved in the design and delivery of toxicology studies.
Senior Ecotoxicologist Bracknell
Skills & Focus: Ecotoxicology, Endocrine Disruption, Data Analysis, Regulatory Compliance, Technical Leadership, CRO Management, Global Strategy, Research Collaboration, Dataset Interpretation, Innovative Strategies
About the Company: A dynamic company specializing in agricultural science and technology.

M3

Medical Writer Abingdon
Skills & Focus: writing, editing, proofreading, content, campaigns, client meetings, planning, design, programme management, medical conferences
About the Company: The Medical Writing team at M3 is responsible for producing a wide variety of content, primarily for Doctors.net.uk, the UK’s largest professional network of d…
Medical Writer Abingdon
Skills & Focus: writing, editing, proofreading, content quality, regulatory compliance, campaign planning, process improvement, strategic input, client meetings, content development
About the Company: M3's Medical Writing team produces a wide variety of content for the healthcare sector, including promotional material, educational modules, and case studies.