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How would you like to be paid for five days but only work four*? Our colleagues’ wellbeing is at the heart of everything we do at OFG, so we’re always looking for new ways to improve everyone’s work/life balance. We’re taking part in a trial of the 4-Day Working Week, meaning that you could be w...

How would you like to be paid for five days but only work four*? Our colleagues’ wellbeing is at the heart of everything we do at OFG, so we’re always looking for new ways to improve everyone’s work/life balance. We’re taking part in a trial of the 4-Day Working Week, meaning that you could be w...

We are a specialised life sciences company focused on advancing innovative treatments for patients with rare and serious medical conditions.With a strong track record in clinical research and regulatory compliance, our team is dedicated to delivering meaningful impact where it's needed most.We ar...

They are currently recruiting a Clinical Negligence Lawyer with 0-3 years PQE to join their Manchester office. This Clinical Negligence Lawyer role will see you handle your own caseload of clinical negligence cases from inception to trial. You must be a qualified solicitor/lawyer with 0-3 years P...

This role involves strategic leadership and execution of medical coding activities for clinical trials, ensuring high-quality coded data that meets industry standards and regulatory requirements. Lead clinical trial coding deliverables and provide mentorship to team members. Develop and implement...

Precision for Medicine is a precision medicine CRO. Precision for Medicine's uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical authorities, advanced biomarker and data analytics solutions, and...

The Lead Clinical Research Associate is a critical core team member responsible for the oversight of a defined set of clinical trial sites within a region. Title: Lead Clinical Research Associate. Demonstrated ability in report writing and strong ability to critically understand clinical research...

The Senior Clinical Trial Manager oversees clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH guidelines, Good Clinical Practices (GCP), and regulatory requirements. They collaborate with the Clinical Project Manager (CPM), CRO representatives, and v...

Proclinical is seeking a Clinical Supply Chain Manager to oversee the management and distribution of clinical trial supplies. Collaborate with clinical managers to determine investigational medicinal product (IMP) needs. Experience in pharmaceutical supply chain management, particularly in clinic...

Join a leading global provider of clinical trial packaging and labelling services as a Project Manager, supporting complex clinical studies for international clients. In this role, you’ll manage timelines, coordinate label design (including booklet labels), and serve as the key liaison between c...

Precision for Medicine is hiring Director, Quality based in Europe. The position can be covered fully remotely from one of our European locations: UK, Spain, Poland, Slovakia, Hungary, Serbia or Romania. Position Summary: The Director, Quality manages the audit program and supports clinical ...

We are seeking a highly experienced Lead Biostatistician for a long-term contract engagement to provide expert statistical leadership on clinical trial projects. You'll be supporting study design, protocol development, and all other statistical aspects of clinical trials. Responsibilitie...

Position Overview: Our client, a public clinical stage well funded biotech is looking for an EU based Medical Director/Senior Medical Director in Clinical Development who will serve as the Clinical Lead for one or more oncology clinical trials. The Medical Director will work with cross-function...

How would you like to be paid for five days but only work four*? Our colleagues’ wellbeing is at the heart of everything we do at OFG, so we’re always looking for new ways to improve everyone’s work/life balance. We’re taking part in a trial of the 4-Day Working Week, meaning that you could ...

Planet Pharma are partnered with a leading pharmaceutical company and we are actively seeking an experienced Senior Manager Regulatory Affairs to join the business on an initial 12 month contract basis. Key Responsibilities: - Shape and implement regional regulatory strategy by advising th...

Job Summary: We are seeking an experienced and driven Senior PK/PD Modeller to join our Clinical Pharmacology team. In this role, you will be responsible for the design, development, and implementation of pharmacokinetic/pharmacodynamic (PK/PD) modeling strategies to support drug development ...

We are seeking a skilled and detail-oriented Law Costs Draftsperson to join our clients growing team to work on a fully remote basis. This is an exciting opportunity for a dedicated Law Costs Draftsperson to work with a dynamic and supportive legal team in a role that offers both flexibility. Th...

About the Role We are seeking a Clinical Data Visualization & Reporting Analyst to support critical functions in clinical trial operations. This role contributes to data-driven decision-making by developing advanced reports and dashboards for medical monitoring, safety review, data quality m...

How would you like to be paid for five days but only work four*? Our colleagues’ wellbeing is at the heart of everything we do at OFG, so we’re always looking for new ways to improve everyone’s work/life balance. We’re taking part in a trial of the 4-Day Working Week, meaning that you could ...

6 month FTC, with possibility to become permanent My client are a fast-growing SaaS company who are mission-led. Their solutions help pharmaceutical, biotechnology, and contract research companies to streamline clinical trial processes. They are looking to appoint a Junior Legal Operatio...

Costs Draftsperson- UK Wide *MUST LIVE IN THE UK* Fully Homebased Full Time & Part Time Available £30,000-£50,000 (Fully negotiable for the right candidate) Bonus scheme available We are proud to be recruiting on behalf of a well-established and highly respected client, who is looking...

Our client is recognised by the legal 500 and is ranked in the 2023 UK Edition for Personal Injury and Clinical Negligence. They are looking to recruit a Solicitor/Legal Executive, ideally with previous multi track/serious injury experience. This role is offered on a permanent basis, Monday...

How would you like to be paid for five days but only work four*? Our colleagues’ wellbeing is at the heart of everything we do at OFG, so we’re always looking for new ways to improve everyone’s work/life balance. We’re taking part in a trial of the 4-Day Working Week, meaning that you could b...

How would you like to be paid for five days but only work four*? Our colleagues’ wellbeing is at the heart of everything we do at OFG, so we’re always looking for new ways to improve everyone’s work/life balance. We’re taking part in a trial of the 4-Day Working Week, meaning that you could b...

Provide administrative support to clinical study teams across multiple trials. Strong understanding of clinical trial processes and regulatory guidelines (ICH-GCP). Proficient in Microsoft Office Suite and clinical trial management systems (CTMS, eTMF).

Summary The Senior Clinical Trial Manager oversees clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH guidelines, Good Clinical Practices (GCP), and regulatory requirements. Experience with clinical trial site start-up and initiation. Senior Clinical...

Strong understanding of clinical trial processes and regulatory guidelines (ICH-GCP). Proficient in Microsoft Office Suite and clinical trial management systems (CTMS, eTMF). We are seeking a detail-oriented and proactive Clinical Trial Assistant (CTA) to join our dynamic team within the Life Sci...

The Senior Clinical Trial Manager oversees clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH guidelines, Good Clinical Practices (GCP), and regulatory requirements. Could you provide direction to ensure consistency in Clinical Operations processes a...

Provide administrative support to clinical study teams across multiple trials. Strong understanding of clinical trial processes and regulatory guidelines (ICH-GCP). Proficient in Microsoft Office Suite and clinical trial management systems (CTMS, eTMF).

The Senior Clinical Trial Manager oversees clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH guidelines, Good Clinical Practices (GCP), and regulatory requirements. Additionally, they may supervise Clinical Trial Managers to ensure deliverables are ...

Strong understanding of clinical trial processes and regulatory guidelines (ICH-GCP). Proficient in Microsoft Office Suite and clinical trial management systems (CTMS, eTMF). We are seeking a detail-oriented and proactive Clinical Trial Assistant (CTA) to join our dynamic team within the Life Sci...

The Senior Clinical Trial Manager oversees clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH guidelines, Good Clinical Practices (GCP), and regulatory requirements. Additionally, they may supervise Clinical Trial Managers to ensure deliverables are ...

The Senior Clinical Trial Manager oversees clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH guidelines, Good Clinical Practices (GCP), and regulatory requirements. Proven ability to build and maintain relationships with clinical trial sites and Pri...