Atkins jobs in LondonCreate job alerts

Your new company Are you a seasoned medical writer with a sharp eye for detail and a deep understanding of clinical development? We're working with a leading international biopharmaceutical company-a pioneer in rare disease innovation-to recruit a Senior Medical Writer to join their high-performing Global Medical Writing team.This is a unique opportunity to contribute to cutting-edge therapies while shaping regulatory and clinical documentation across all phases of drug development. Your new role As a Senior Medical Writer, you'll be responsible for authoring and managing a wide range of regulatory and clinical documents, from protocols and study reports to briefing books and eCTD modules. You'll collaborate with cross-functional teams, lead document strategy, and ensure content meets global regulatory standards. Key Responsibilities Author and edit clinical study documentation: protocols, amendments, ICFs, CSRs Prepare regulatory documents including Investigator's Brochures, PBRERs, DSURs, INDs, and NDA/BLA components. Lead document planning, timelines, and review cycles across study teams Represent Medical Writing in cross-functional meetings and development teams Provide peer review and editorial support across regulatory deliverablesContribute to the development of templates and best practices within Medical Writing and beyond Ensure compliance with internal SOPs and global regulatory standards What you'll need to succeed Bachelor's degree or higher in a scientific discipline Formal training or certification in medical writing (e.g., AMWA, DIA) is highly desirable. Expert medical writing experience in pharma/biotech Strong track record of authoring documents across all phases of clinical development Experience with INDs, NDAs/BLAs, PBRERs, DSURs, and regulatory briefing books Familiarity with eCTD structure and integrated summaries (ISS/ISE) Advanced understanding of clinical research, biostatistics, and regulatory frameworks Proficiency in Microsoft Office Suite, Adobe Acrobat, and document management systems (e.g., Veeva, SharePoint) Strong project leadership and stakeholder management skills Excellent written and verbal communication with the ability to translate complex science into clear, compliant documentation What you'll get in return Work with a globally recognised biotech innovator Be part of a collaborative, science-driven culture Hybrid working model with flexibility and autonomy Competitive package with long-term career development What you need to do now Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and residing in the UK. If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Roberta Atkins on 03330106292

Your new company Are you a detail-driven communicator with a passion for science and clinical research? We're partnering with a leading global biopharmaceutical company-renowned for its innovation in rare disease therapies-to find a Medical Writer to join their Clinical Development team.This is a fantastic opportunity for someone looking to grow their career in medical writing within a collaborative, science-led environment that values precision, clarity, and impact. Your new role As a Medical Writer, you'll play a key role in the development and delivery of high-quality clinical documentation that supports regulatory submissions and scientific publications. You'll work cross-functionally with clinical teams, statisticians, and regulatory experts to ensure documents are accurate, compliant, and aligned with strategic goals. Key Responsibilities: Draft and edit clinical study documents including protocols, amendments, informed consent forms, and study reports Contribute to safety and efficacy documentation such as Investigator's Brochures and periodic safety reports (PBRERs, DSURs) Manage timelines, meetings, and review cycles for document development Provide peer review and editing support across regulatory documentation Support the development of templates and best practices within the medical writing function Collaborate effectively across clinical, regulatory, and safety teams What you'll need to succeed Bachelor's degree or higher (scientific discipline preferred) Certifications such as AMWA or DIA are highly regarded. Experience in medical writing within pharma or biotech Familiarity with clinical trial documentation, protocol design, and regulatory standards Strong grasp of biostatistics, clinical data interpretation, and medical terminology Proficiency in Microsoft Office Suite and document management systems (e.g., Veeva, SharePoint) Exceptional written and verbal communication Strong project management and organisational skills Ability to work independently and manage multiple priorities Detail-oriented with a proactive mindset What you'll get in return Work with a pioneering biotech company making a real difference in patient lives. Be part of a high-performing, supportive team with clear career development pathways. Hybrid working model with flexibility and autonomy Competitive salary and benefits package What you need to do now Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and residing in the UK. If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Roberta Atkins on 03330106292

IT and Digital Skills Trainer – Remote (1 Day/Month in Central London) Salary: £35,000 – £45,000 | Full-Time | 25 Days Holiday + Bank Holidays Are you passionate about equipping learners with the digital skills they need to thrive in today’s tech-driven world? We’re working with a nationally recognised training provider with over 20 years’ experience in delivering apprenticeships and vocational training. Supporting over 12,000 learners each year and holding an impressive 91% employer satisfaction rating, they are at the forefront of shaping digital talent across the UK. They are now looking for an enthusiastic and experienced IT and Digital Skills Trainer to join their team and deliver high-quality learning across Level 2 IT and digital programmes. What’s on Offer: • Salary: £35,000 – £40,000 per annum, • Hours: 37.5 hours per week, • Location: Primarily remote with just 1 day per month in Central London, • Holidays: 25 days plus bank holidays, • Development: Ongoing training and real opportunities for career progression Key Responsibilities: • Deliver engaging, interactive training sessions across a variety of digital topics such as:, • Cybersecurity, • Computer Programming, • Digital Graphics, • Spreadsheets, • Networks, • IT Support, • Digital Skills Projects, • Data Handling and Security, • Presentations and Communication, • Conduct initial assessments to identify learner needs and tailor support appropriately, • Guide and mentor learners throughout their programme, supporting progression and achievement, • Maintain accurate records, monitor learner progress, and ensure compliance with quality standards, • Work collaboratively with internal teams to ensure consistent, high-quality delivery ✅ What We’re Looking For: • Teaching Qualification: PGCE, CertEd, or Level 4+ (Level 3 accepted if working towards Level 4), • Experience: Proven background in delivering remote IT and digital skills training, • Industry Knowledge: Practical IT or digital sector experience with relevant certifications, • Skills: Strong organisational and time-management skills, with a commitment to safeguarding and high-quality education, • Essential: Experience delivering apprenticeships or adult education training programmes in a group setting, • Desirable: Full UK driving licence and access to a vehicle (occasional travel may be required) Interested? Contact Simon Atkins at Newcastle Pertemps on 07894 752230 to find out more or apply today.

Your new company Are you a senior-level medical writing professional ready to take the lead on global clinical documentation strategy? We're working with a top-tier international biopharmaceutical company-a trailblazer in rare disease innovation-to recruit a Principal Clinical Medical Writer to join their Clinical Development function.This is a high-impact role offering strategic oversight, cross-functional leadership, and the opportunity to shape regulatory documentation across multiple programs and therapeutic areas. Your new role As Principal Clinical Medical Writer, you'll be responsible for leading the medical writing effort across clinical development programs, managing timelines, mentoring writers, and ensuring the delivery of high-quality, compliant documentation for global regulatory submissions.You'll work closely with the Head of Medical Writing and cross-functional teams to drive consistency, efficiency, and excellence in clinical content. Key Responsibilities • Provide functional oversight and mentorship to medical writing staff, • Lead the development of clinical and regulatory documents including protocols, CSRs, IBs, PBRERs, DSURs, and briefing books, • Manage timelines, resources, and review cycles across multiple programs, • Represent Medical Writing in cross-functional meetings and strategic planning sessions, • Support regulatory submissions (INDs, NDAs, BLAs) including eCTD Modules 2 & 5, ISS/ISE, • Contribute to process improvement and template development across departments, • Master's degree or higher in a scientific discipline preferred, • Formal training or certification in medical writing (e.g., AMWA, EMWA, DIA) is highly desirable., • Expert experience of medical writing in pharma/biotech, • Proven leadership in managing writing teams or projects, • Strong track record of authoring documents across all phases of drug development, • Experience with INDs, NDAs/BLAs, periodic safety documents, and regulatory briefing books, • Familiarity with eCTD structure and integrated summaries (ISS/ISE), • Advanced understanding of clinical research, biostatistics, and regulatory frameworks, • Proficiency in Microsoft Office Suite, Adobe Acrobat, MS Project, and document management systems (e.g., Veeva, SharePoint), • Excellent project management and stakeholder engagement skills, • Join a globally recognised biotech innovator with a strong pipeline, • Lead strategic initiatives and mentor a high-performing team, • Hybrid working model with flexibility and autonomy If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Roberta Atkins on 03330106292

We are seeking a Senior or Principal Waste Management Consultant to play a key role in the Atkins Waste and Resource Management business.