Clinical Project Leader - Bio
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This document is a job posting for a Clinical Project Leader position at a biopharmaceutical company focused on developing therapies for allergies. The posting provides details on the responsibilities, which include project management of clinical studies in Europe and North America to ensure on-time and on-budget completion, as well as management of third party suppliers and study documents. Qualifications sought include a life sciences degree, minimum 6 years of clinical research experience including strong project management skills, and knowledge of international regulations and good clinical practices.
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CTC Resourcing Solutions is a staffing organization providing flexible resourcing to the pharmaceutical industry across Europe, with placements in clinical development, data management, regulatory affairs, and medical marketing. They are currently looking for a Clinical Research Associate for field-based work in the UK. The position involves site monitoring, management, and ensuring protocol and regulatory adherence. Qualifications include a bachelor's degree in a health field, 1+ years of monitoring experience, strong communication skills, and ability to manage priorities and relationships. The offer includes a competitive salary, company car, bonus, and flexible benefits package.Program Operation Manager - Basel, Switzerland
Program Operation Manager - Basel, SwitzerlandVania Macario
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CTC Resourcing Solutions is a staffing organization based in Basel, London, and Munich providing flexible resourcing solutions to the pharmaceutical industry across Europe. They are currently looking for a Program Operation Manager based in Basel, Switzerland to support clinical teams and designated programs. The Program Operation Manager will plan and track external program resources and internal resources, ensure operational and financial excellence, provide operational guidance and leadership for assigned clinical programs, and ensure compliance with operational processes. Qualifications include a Bachelor's degree in life science or business administration, 5-7 years of pharmaceutical industry experience in clinical research or finance, strong clinical operations and financial background, and fluency in English.Senior Biostatistician - Switzerland, Germany or UK
Senior Biostatistician - Switzerland, Germany or UKVania Macario
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CTC Resourcing Solutions is a specialist staffing organization providing flexible resourcing to the pharmaceutical industry across Europe. They are currently looking for a Senior Biostatistician based in Switzerland, Germany, or the UK. The position involves leading statistical aspects of clinical trials including design, analysis, and results interpretation. Key responsibilities include ensuring quality and timeliness of deliverables, tracking milestones, adhering to regulations, and communicating results. Qualifications required include a university degree in mathematics, statistics, or related field, proven experience in all tasks of a trial statistician, experience with clinical research and regulations, proficiency in statistical software, strong communication and organizational skills, and fluency in English. The offer includes a competitive salary andSenior Medical Writer - UK
Senior Medical Writer - UKVania Macario
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CTC Resourcing Solutions is a specialist staffing organization based in Basel, London, and Munich providing flexible staffing to the pharmaceutical industry across Europe. They are currently looking for a Senior Medical Writer to be based in Berkshire, England, West Lothian, Scotland, or home-based. The role would involve leading global writing teams to develop clinical trial documents for drugs and medical devices. Qualifications include a science degree, medical writing experience, and experience preparing clinical study protocols and reports. The successful candidate would receive a competitive salary and benefits package.Manager drug safety training emea 69 855-mdst-w
Manager drug safety training emea 69 855-mdst-wAndrew Webb
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This document provides information about a permanent Manager Drug Safety Training position in Switzerland or the UK. The responsibilities include developing and providing drug safety training to new and current staff. Qualifications sought are a nursing, pharmacy, or science background with 4 years of drug safety experience, knowledge of European drug safety legislation, training experience, and strong communication skills. Those interested should send a CV and application quoting reference number 69-855-MDST-W to the provided recruitment contact information.Medical liaison manager 69 850-mlm-w
Medical liaison manager 69 850-mlm-wAndrew Webb
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CTC Resourcing Solutions is a specialist staffing agency providing flexible resourcing to the pharmaceutical industry. They are seeking a Medical Liaison Manager located in South England for a client. The client is an integrated biopharmaceutical company advancing novel cancer and inflammatory disease therapies. As Medical Liaison Manager, responsibilities include developing relationships with healthcare professionals, responding to information requests, coordinating investigator initiated trials, providing scientific training and medical insight, and identifying potential clinical trial sites. Qualifications include medical or scientific experience, excellent communication skills, strong project management and medical affairs experience, and knowledge of the NHS. The offer includes a competitive salary, bonus, benefits, and stock options.Clinical study manager 62 944-csm-w
Clinical study manager 62 944-csm-wAndrew Webb
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CTC Resourcing Solutions is a European staffing agency providing flexible resourcing to the pharmaceutical industry, including clinical development, data management, and regulatory affairs roles. They are seeking a Clinical Study Manager for a 6-month contract with a UK pharmaceutical client. The role involves managing ongoing oncology studies in Europe, ensuring delivery according to regulations and timelines while overseeing contract research organizations. Qualified candidates will have a science degree, 3-5 years of clinical research experience preferably including time as a clinical research associate, and skills in relationship building, influencing, and managing vendors.Senior clinical research associate field based, uk
Senior clinical research associate field based, ukAndrew Webb
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CTC Resourcing Solutions is a specialist staffing organization providing flexible resourcing solutions to the pharmaceutical industry across Europe. They are currently looking for a Senior Clinical Research Associate for a field-based role in the UK. The client is a leading provider of biopharmaceutical services with a global network helping develop and commercialize top drugs. Responsibilities include site selection, monitoring, and management for clinical trials. Qualifications required are a scientific degree and at least two years of monitoring experience. The offer includes a competitive salary, bonus, and flexible benefits package.Associate manager, global risk management emea 69 869-amgrm-w
Associate manager, global risk management emea 69 869-amgrm-wAndrew Webb
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The document advertises an Associate Manager, Global Risk Management position at a biopharmaceutical company located in West London. The role involves managing risk data and documents, tracking country launch readiness, supporting training materials, and monitoring risk minimization programs. Qualifications include a minimum of 2 years industry experience in drug safety, risk management programs, and global regulatory requirements. The position offers a competitive salary, bonus, and benefits.Senior Fellow
Senior FellowVania Macario
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CTC Resourcing Solutions is a pan-European staffing firm providing flexible resourcing to the pharmaceutical industry. They are seeking a Senior Fellow based in Basel, Switzerland to support oncology drug development through clinical pharmacology, pharmacometrics, and pharmacokinetic expertise. Responsibilities include designing clinical strategies, performing analyses, contributing to documents, collaborating cross-functionally, and mentoring others. Requirements include a PhD or PharmD, 6-10 years of relevant experience, expertise in pharmacometric tools and related disciplines, strong communication and project management skills, and fluency in English. The offer includes a competitive salary and package as well as career opportunities.Clinical Project Leader - Bio
- 1. Should you be interested in the above position and wish to apply, please send your application with your CV, quoting the above reference number, to our recruitment team at recruitment@ctcon.ch CTC Resourcing Solutions, 117 Waterloo Road, SE1 8UL, London, UK Tel.: +44 207 193 9972 www.ctcresourcing.com info@ctcon.ch Providing Flexible Resourcing Solutions CTC Resourcing Solutions, founded 1997, is a pan-European specialist staffing organisation with offices in London, Basel and Munich, providing flexible resourcing solutions to the pharmaceutical industry across Europe, with contract and permanent placements in clinical development, data management, statistics, regulatory affairs and medical marketing For a key client, we are currently looking for a: Clinical Project Leader Reference Number: 893073-W Type of placement: Contract or Permanent Location: Oxfordshire, UK Our client is an independent clinical-stage biopharmaceutical company focused on developing a portfolio of therapies for the treatment of allergies. With several treatments currently in development, a number of products are in early-stage stage trials with the most advanced compound currently in phase III. The company requires an experienced Clinical Study Manager to lead a programme of outsourced international trials with accountability for the budget, timelines, quality and reporting of allocated studies. This is an exciting opportunity to work for a young and progressive company whose ultimate ambition is to build a successful immunotherapy company, improving patients’ lives around the world. Main Responsibilities:  Project Management of all clinical aspects of clinical studies (all phases) in Europe and North America to ensure successful completion of clinical studies on time and within budget.  Management of third party suppliers.  Review of monitoring reports, study plans (DMP, SAP, project plan, etc).  Review and/or preparation of protocols, Investigator Brochures, Clinical Study Reports.  Attendance at Investigator meetings, Site Initiation Visits.  Co-monitoring with CRO CRAs. Qualifications and Experience:  Bachelor’s degree or equivalent in a biomedical or life sciences discipline  Demonstrated study management experience in clinical or pharmaceutical development  Minimum 6 years’ experience in clinical research, with strong Clinical Project Management experience.  Competence to identify challenges and risks and suggest/implement appropriate actions.  Experience in maintenance of study timelines and vendor management activities.  Experience in managing all aspects of clinical studies and clinical development  Working knowledge of international regulatory and ICH GCP guidelines  Highly effective verbal and written communication/presentation skills in English.