Company Detail

Job Openings

• 

  Regulatory Analyst  

  MastarRec

  [fulltime] - London

  Posted: 01/12/2025

  Apply Now

  Job DescriptionDescription:Our prestigious client is seeking an experi... Read More

  Job Description
  Description:
  Our prestigious client is seeking an experienced Regulatory Analyst to join a fast-paced, innovation-driven biotechnology client. This role focuses on ensuring compliance with international regulatory requirements. For product development, clinical trials, and commercialization processes in the healthcare or life sciences sector.
  The successful candidate will be responsible for compiling, reviewing, and submitting documentation to regulatory authorities and maintaining up-to-date knowledge of changing industry standards.
  Key Responsibilities:
  Prepare, submit, and track regulatory filings such as INDs, NDAs, CTAs, and amendments.
  Ensure compliance with FDA, EMA, MHRA, and other global regulatory agencies.
  Monitor legislative and regulatory changes affecting product development and advise stakeholders.
  Collaborate with R&D, clinical, and legal teams to compile documentation for approvals.
  Maintain regulatory documentation databases and assist in audits or inspections.
  Support product labelling reviews and ensure proper documentation for promotional material approvals.
  Provide input on regulatory strategies during product lifecycle stages.
  
  
  RequirementsRequired Skills:
  Strong understanding of EU and FDA regulatory frameworks and submission processes.
  Experience working with regulatory submission platforms (e.g., eCTD).
  Excellent technical writing, documentation, and communication skills.
  Ability to manage multiple projects with attention to deadlines and compliance.
  High level of attention to detail and analytical thinking.
  
  Desired Skills:
  Experience in biotechnology or pharmaceutical regulatory consulting.
  Familiarity with medical device regulations (MDR, IVDR).
  Knowledge of ICH guidelines, GxP, and ISO standards.
  
  
  BenefitsJob Benefits:
  Competitive base salary & performance bonus
  Hybrid working flexibility
  25 days annual leave + bank holidays
  Private medical insurance
  Professional development and certification support
  Inclusive, growth-oriented company culture
  
  
  
  Requirements
  Required Skills Deep knowledge of digital payment ecosystems, architectures, and technologies Expertise in payment gateway integration, tokenisation, and fraud detection systems Strong understanding of ISO 20022, EMV, NFC, and 3D Secure protocols Familiarity with cloud-native architecture (AWS, GCP, or Azure) Ability to document and present technical concepts to stakeholders clearly Desired Skills Experience with real-time payment systems and blockchain-based solutions Hands-on coding experience with Java, Python, or Node.js TOGAF or AWS Solution Architect certification preferred Knowledge of financial data orchestration and embedded finance architectures Read Less

  Apply Now
• 

  Regulatory Analyst  

  MastarRec

  [fulltime] - London

  Posted: 01/12/2025

  Apply Now

  Job DescriptionDescription:Our prestigious client is seeking an experi... Read More

  Job Description
  Description:
  Our prestigious client is seeking an experienced Regulatory Analyst to join a fast-paced, innovation-driven biotechnology client. This role focuses on ensuring compliance with international regulatory requirements. For product development, clinical trials, and commercialization processes in the healthcare or life sciences sector.
  The successful candidate will be responsible for compiling, reviewing, and submitting documentation to regulatory authorities and maintaining up-to-date knowledge of changing industry standards.
  Key Responsibilities:
  Prepare, submit, and track regulatory filings such as INDs, NDAs, CTAs, and amendments.
  Ensure compliance with FDA, EMA, MHRA, and other global regulatory agencies.
  Monitor legislative and regulatory changes affecting product development and advise stakeholders.
  Collaborate with R&D, clinical, and legal teams to compile documentation for approvals.
  Maintain regulatory documentation databases and assist in audits or inspections.
  Support product labelling reviews and ensure proper documentation for promotional material approvals.
  Provide input on regulatory strategies during product lifecycle stages.
  
  
  RequirementsRequired Skills:
  Strong understanding of EU and FDA regulatory frameworks and submission processes.
  Experience working with regulatory submission platforms (e.g., eCTD).
  Excellent technical writing, documentation, and communication skills.
  Ability to manage multiple projects with attention to deadlines and compliance.
  High level of attention to detail and analytical thinking.
  
  Desired Skills:
  Experience in biotechnology or pharmaceutical regulatory consulting.
  Familiarity with medical device regulations (MDR, IVDR).
  Knowledge of ICH guidelines, GxP, and ISO standards.
  
  
  BenefitsJob Benefits:
  Competitive base salary & performance bonus
  Hybrid working flexibility
  25 days annual leave + bank holidays
  Private medical insurance
  Professional development and certification support
  Inclusive, growth-oriented company culture
  
  
  
  Requirements
  Required Skills Deep knowledge of digital payment ecosystems, architectures, and technologies Expertise in payment gateway integration, tokenisation, and fraud detection systems Strong understanding of ISO 20022, EMV, NFC, and 3D Secure protocols Familiarity with cloud-native architecture (AWS, GCP, or Azure) Ability to document and present technical concepts to stakeholders clearly Desired Skills Experience with real-time payment systems and blockchain-based solutions Hands-on coding experience with Java, Python, or Node.js TOGAF or AWS Solution Architect certification preferred Knowledge of financial data orchestration and embedded finance architectures Read Less

  Apply Now
• 

  Regulatory Affairs Specialist  

  MastarRec

  [fulltime] - London

  Posted: 01/12/2025

  Apply Now

  Job DescriptionJob DescriptionWe are seeking a highly skilled and deta... Read More

  Job Description
  Job Description
  We are seeking a highly skilled and detail-oriented Regulatory Affairs Specialist to join a leading life sciences and medical technology organization. In this pivotal role, you will support the development, submission, and maintenance of regulatory documentation for clinical trials, product registration, and post-market surveillance activities in accordance with FDA, EMA, MHRA, and other global regulatory bodies.
  This is an excellent opportunity for someone looking to contribute to regulatory strategy, gain cross-functional exposure, and work on cutting-edge biotech or medical device products within a fast-paced regulatory environment.
  Job Responsibilities
  Prepare, compile, and submit regulatory documentation (INDs, CTAs, 510(k), CE marking, etc.)
  Ensure regulatory compliance with FDA, EMA, MHRA, ISO, and ICH guidelines
  Collaborate with R&D, Clinical Affairs, and Quality Assurance teams to ensure product readiness
  Maintain regulatory files, technical documentation, and product registrations across global markets
  Monitor regulatory changes and provide guidance to internal stakeholders
  Support internal and external audits and inspections
  Assist with labelling review, risk assessments, and post-market surveillance
  
  
  RequirementsRequired Skills
  Strong understanding of global regulatory requirements (FDA, EMA, MHRA, ISO 13485)
  Excellent written and verbal communication skills
  Experience preparing and submitting dossiers and regulatory filings
  Detail-oriented with strong documentation and project tracking skills
  Proficiency with Microsoft Office and regulatory software systems
  
  Desired Skills
  Regulatory Affairs Certification (RAC) is a plus
  Experience in regulatory submissions for medical devices, diagnostics, or biotech products
  Knowledge of eCTD publishing tools and regulatory information management systems (RIMS)
  Ability to interpret technical documentation and scientific data
  
  
  BenefitsJob Benefits
  Competitive salary with performance-based bonuses
  Private health and dental insurance
  Annual training and certification reimbursement
  25 days holiday + bank holidays
  Hybrid working model and flexible scheduling
  Career advancement in a growing regulatory team
  
  
  
  Requirements
  Required Skills Strong proficiency in CRISPR/Cas9 genome editing Molecular cloning, PCR, gel electrophoresis, and sequencing Experience working with mammalian and bacterial cell lines Familiarity with LIMS and laboratory data management tools Excellent documentation and scientific communication skills Desired Skills PhD or MSc in Genetics, Molecular Biology, or Biomedical Engineering Experience in bioinformatics tools (e.g., BLAST, Geneious, Benchling) Knowledge of synthetic biology or mRNA therapeutics Published peer-reviewed scientific research in the field Read Less

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• 

  Bioinformatics Scientist  

  MastarRec

  [fulltime] - Oxford

  Posted: 01/12/2025

  Apply Now

  Job DescriptionOur clients are hiring a results-driven Bioinformatics... Read More

  Job Description
  Our clients are hiring a results-driven Bioinformatics Analyst to contribute to high-impact biomedical research projects by analysing complex genomic and multi-omics data. The ideal candidate will have a strong foundation in biological data science, programming, and algorithmic thinking, along with experience working in a cross-functional life sciences or healthcare setting.
  
  Process, analyse, and interpret large-scale datasets including genomic, transcriptomics, proteomic, and clinical data.
  Perform data integration and pipeline development using scripting languages like Python, R, or Perl.
  Develop and optimize bioinformatics workflows for sequencing data (e.g., RNA-seq, WES, WGS).
  Use tools such as GATK, Bioconductor, BWA, SAMtools, and other NGS pipelines.
  Collaborate with biologists, clinicians, and data scientists to generate actionable insights.
  Maintain detailed documentation and ensure data analysis meets reproducibility standards.
  Contribute to publications, reports, and presentations for internal and external stakeholders.
  
  
  RequirementsProven experience in bioinformatics analysis of high-throughput sequencing data (e.g., NGS).
  Proficiency with Python, R, and command-line tools in Linux/Unix environments.
  Familiarity with cloud platforms (e.g., AWS, Google Cloud) and HPC environments.
  Strong understanding of molecular biology, genetics, and biostatistics.
  Excellent problem-solving skills and attention to detail.
  Strong written and verbal communication skills to support collaborative research.
  
  Desired Skills:
  Experience with machine learning applications in bioinformatics.
  Background in single-cell RNA sequencing, epigenomics, or meta-genomics.
  Knowledge of FAIR data principles and version control systems (e.g., Git).
  Understanding of clinical bioinformatics and regulatory-compliant environments.
  
  
  BenefitsCompetitive salary and annual performance bonus
  Hybrid working model with flexible hours
  Private healthcare and dental cover
  Generous annual leave and training budget
  Access to cutting-edge tools and industry-leading biotech partners
  
  
  
  Requirements
  Required Skills Strong proficiency in CRISPR/Cas9 genome editing Molecular cloning, PCR, gel electrophoresis, and sequencing Experience working with mammalian and bacterial cell lines Familiarity with LIMS and laboratory data management tools Excellent documentation and scientific communication skills Desired Skills PhD or MSc in Genetics, Molecular Biology, or Biomedical Engineering Experience in bioinformatics tools (e.g., BLAST, Geneious, Benchling) Knowledge of synthetic biology or mRNA therapeutics Published peer-reviewed scientific research in the field Read Less

  Apply Now
• 

  Clinical Trials, FDA, EMA Compliance  

  MastarRec

  [fulltime] - London

  Posted: 01/12/2025

  Apply Now

  Job DescriptionJob DescriptionWe are seeking a highly skilled and deta... Read More

  Job Description
  Job Description
  We are seeking a highly skilled and detail-oriented Regulatory Affairs Specialist to join a leading life sciences and medical technology organization. In this pivotal role, you will support the development, submission, and maintenance of regulatory documentation for clinical trials, product registration, and post-market surveillance activities in accordance with FDA, EMA, MHRA, and other global regulatory bodies.
  This is an excellent opportunity for someone looking to contribute to regulatory strategy, gain cross-functional exposure, and work on cutting-edge biotech or medical device products within a fast-paced regulatory environment.
  Job Responsibilities
  Prepare, compile, and submit regulatory documentation (INDs, CTAs, 510(k), CE marking, etc.)
  Ensure regulatory compliance with FDA, EMA, MHRA, ISO, and ICH guidelines
  Collaborate with R&D, Clinical Affairs, and Quality Assurance teams to ensure product readiness
  Maintain regulatory files, technical documentation, and product registrations across global markets
  Monitor regulatory changes and provide guidance to internal stakeholders
  Support internal and external audits and inspections
  Assist with labelling review, risk assessments, and post-market surveillance
  
  
  RequirementsRequired Skills
  Strong understanding of global regulatory requirements (FDA, EMA, MHRA, ISO 13485)
  Excellent written and verbal communication skills
  Experience preparing and submitting dossiers and regulatory filings
  Detail-oriented with strong documentation and project tracking skills
  Proficiency with Microsoft Office and regulatory software systems
  
  9. Desired Skills
  Regulatory Affairs Certification (RAC) is a plus
  Experience in regulatory submissions for medical devices, diagnostics, or biotech products
  Knowledge of eCTD publishing tools and regulatory information management systems (RIMS)
  Ability to interpret technical documentation and scientific data
  
  
  BenefitsJob Benefits
  Competitive salary with performance-based bonuses
  Private health and dental insurance
  Annual training and certification reimbursement
  25 days holiday + bank holidays
  Hybrid working model and flexible scheduling
  Career advancement in a growing regulatory team
  
  
  
  Requirements
  Required Skills In-depth knowledge of GCP, clinical research regulations, and ethical standards Experience with clinical data collection, source documentation, and informed consent processes Proficiency with electronic data capture systems (e.g., REDCap, Medidata, or similar) Strong organizational and time management skills Excellent communication and interpersonal abilities Detail-oriented and able to handle multiple trials simultaneously Desired Skills Bachelor’s degree in Life Sciences, Nursing, or Health Sciences ACRP or SOCRA certification Previous experience in oncology, cardiology, or rare disease clinical trials Familiarity with clinical trial software platforms and regulatory submissions Read Less

  Apply Now
• 

  Regulatory Affairs Specialist  

  MastarRec

  [fulltime] - London

  Posted: 01/12/2025

  Apply Now

  Job DescriptionJob DescriptionWe are seeking a highly skilled and deta... Read More

  Job Description
  Job Description
  We are seeking a highly skilled and detail-oriented Regulatory Affairs Specialist to join a leading life sciences and medical technology organization. In this pivotal role, you will support the development, submission, and maintenance of regulatory documentation for clinical trials, product registration, and post-market surveillance activities in accordance with FDA, EMA, MHRA, and other global regulatory bodies.
  This is an excellent opportunity for someone looking to contribute to regulatory strategy, gain cross-functional exposure, and work on cutting-edge biotech or medical device products within a fast-paced regulatory environment.
  Job Responsibilities
  Prepare, compile, and submit regulatory documentation (INDs, CTAs, 510(k), CE marking, etc.)
  Ensure regulatory compliance with FDA, EMA, MHRA, ISO, and ICH guidelines
  Collaborate with R&D, Clinical Affairs, and Quality Assurance teams to ensure product readiness
  Maintain regulatory files, technical documentation, and product registrations across global markets
  Monitor regulatory changes and provide guidance to internal stakeholders
  Support internal and external audits and inspections
  Assist with labelling review, risk assessments, and post-market surveillance
  
  
  RequirementsRequired Skills
  Strong understanding of global regulatory requirements (FDA, EMA, MHRA, ISO 13485)
  Excellent written and verbal communication skills
  Experience preparing and submitting dossiers and regulatory filings
  Detail-oriented with strong documentation and project tracking skills
  Proficiency with Microsoft Office and regulatory software systems
  
  Desired Skills
  Regulatory Affairs Certification (RAC) is a plus
  Experience in regulatory submissions for medical devices, diagnostics, or biotech products
  Knowledge of eCTD publishing tools and regulatory information management systems (RIMS)
  Ability to interpret technical documentation and scientific data
  
  
  BenefitsJob Benefits
  Competitive salary with performance-based bonuses
  Private health and dental insurance
  Annual training and certification reimbursement
  25 days holiday + bank holidays
  Hybrid working model and flexible scheduling
  Career advancement in a growing regulatory team
  
  
  
  Requirements
  Required Skills Strong proficiency in CRISPR/Cas9 genome editing Molecular cloning, PCR, gel electrophoresis, and sequencing Experience working with mammalian and bacterial cell lines Familiarity with LIMS and laboratory data management tools Excellent documentation and scientific communication skills Desired Skills PhD or MSc in Genetics, Molecular Biology, or Biomedical Engineering Experience in bioinformatics tools (e.g., BLAST, Geneious, Benchling) Knowledge of synthetic biology or mRNA therapeutics Published peer-reviewed scientific research in the field Read Less

  Apply Now
• 

  Full Stack Engineer  

  MastarRec

  [fulltime] - London

  Posted: 01/12/2025

  Apply Now

  Job DescriptionWe’re hiring a talented and experienced Backend / Full... Read More

  Job Description
  We’re hiring a talented and experienced Backend / Full Stack Engineer to join an agile product development team working on modern web applications and scalable platforms. You’ll be responsible for building, maintaining, and optimising server-side logic and APIs, and contributing to full-stack solutions using JavaScript/TypeScript, Node.js, and React.
  This is an opportunity to work in a fast-moving environment. Where innovation, reliability, and clean code are valued, supporting products within FinTech, Healthcare Technology, or SaaS ecosystems.
  
  Job Responsibilities
  Design, build, and maintain scalable server-side applications and RESTful APIs using Node.js, Express, or similar frameworks.
  Collaborate with frontend engineers to build seamless integrations using React.js or similar JavaScript frameworks.
  Write clean, well-tested, and documented code that adheres to modern development best practices.
  Implement CI/CD pipelines and ensure reliable code deployment and integration.
  Work cross-functionally with Product Managers, Designers, and QA to ship high-quality features.
  Optimize system performance, troubleshoot production issues, and participate in code reviews.
  Contribute to architectural decisions and refactor legacy systems when required.
  
  
  RequirementsRequired Skills
  Strong hands-on experience with Node.js, Express, and API development
  Proficiency in JavaScript/TypeScript
  Solid understanding of SQL/NoSQL databases (e.g., PostgreSQL, MongoDB)
  Experience with CI/CD pipelines and containerization (Docker)
  Experience building and consuming RESTful or GraphQL APIs
  Familiarity with version control tools (e.g., Git, GitHub)
  
  Desired Skills
  Frontend development experience with React.js, Next.js, or similar
  Cloud deployment experience (AWS, Azure, GCP)
  Experience in micro services architecture
  Familiarity with Agile methodologies and TDD
  Prior experience in FinTech, Healthcare, or SaaS is a plus
  
  
  BenefitsJob Benefits
  Competitive salary and performance bonuses
  Private health insurance and wellness support
  Remote-first policy with flexible working hours
  Learning & development allowance
  Equity / stock options (depending on client)
  Modern tech stack, collaborative team culture
  
  
  Read Less

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• 

  GRC Consultant  

  MastarRec

  [fulltime] - London

  Posted: 01/12/2025

  Apply Now

  Job DescriptionWe are seeking an experienced GRC Consultant to support... Read More

  Job Description
  We are seeking an experienced GRC Consultant to support and advise clients in managing cyber risks, ensuring compliance with industry standards, and implementing robust information security governance frameworks. You will work across multiple sectors, helping clients improve their risk posture through audit readiness, control assessments, policy development, and regulatory compliance.
  The ideal candidate will have deep knowledge of security. frameworks (ISO 27001, NIST, CIS), regulatory mandates (GDPR, DORA, PCI DSS), and a strategic approach to enterprise-level governance and risk programs.
  Job Responsibilities
  Advise clients on cybersecurity governance, risk management, and compliance frameworks
  Perform risk assessments, control gap analyses, and audits (ISO 27001, SOC 2, etc.)
  Develop and implement information security policies, procedures, and risk registers
  Lead client engagements related to GDPR, DORA, and other regulatory requirements
  Support third-party vendor risk assessments and due diligence activities
  Prepare reports and recommendations for CISO, board, and audit committee presentations
  Contribute to certification readiness and internal audit programs
  Collaborate with technical teams to align risk controls with business strategy
  
  
  RequirementsRequired Skills
  In-depth knowledge of ISO 27001, NIST CSF, GDPR, and risk management frameworks
  Experience performing security risk assessments, internal audits, and compliance reviews
  Strong understanding of cybersecurity controls, regulatory mandates, and business risk alignment
  Excellent client communication, stakeholder management, and reporting skills
  Familiarity with GRC platforms (e.g., RSA Archer, ServiceNow GRC, LogicGate)
  
  Desired Skills
  Certifications such as CISM, CRISC, ISO 27001 Lead Auditor, or similar
  Experience working with financial services, healthcare, or SaaS industries
  Understanding of emerging regulations (e.g., DORA, NIS2, AI Act)
  Cloud compliance knowledge (e.g., CSA CCM, AWS/Azure/GCP compliance)
  Familiarity with SOC 2, PCI DSS, HIPAA frameworks
  
  
  BenefitsCompetitive salary with performance-based bonus
  Private healthcare & pension scheme
  Hybrid or remote work options
  Ongoing professional development and certification support (CISM, CRISC, ISO Lead Auditor)
  25+ days annual leave
  Access to cybersecurity conferences and industry events
  
  
  
  Requirements
  Required Skills In-depth knowledge of ISO 27001, NIST CSF, GDPR, and risk management frameworks Experience performing security risk assessments, internal audits, and compliance reviews Strong understanding of cybersecurity controls, regulatory mandates, and business risk alignment Excellent client communication, stakeholder management, and reporting skills Familiarity with GRC platforms (e.g., RSA Archer, ServiceNow GRC, LogicGate) Desired Skills Certifications such as CISM, CRISC, ISO 27001 Lead Auditor, or similar Experience working with financial services, healthcare, or SaaS industries Understanding of emerging regulations (e.g., DORA, NIS2, AI Act) Cloud compliance knowledge (e.g., CSA CCM, AWS/Azure/GCP compliance) Familiarity with SOC 2, PCI DSS, HIPAA frameworks Read Less

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• 

  Part-Time Work Experience Placement (Sales / Marketing / Management / HR Graduate)  

  MastarRec

  [parttime] - London

  Posted: 01/12/2025

  Apply Now

  Job DescriptionLocationRemote (travel to client sites when required –... Read More

  Job Description
  Location
  Remote (travel to client sites when required – expenses covered)
  Type
  Part-Time Work Experience (Unpaid; travel expenses reimbursed)
  About the Role
  We’re offering a valuable work experience. Opportunity for a recent university graduate with a degree in Sales, Marketing & Management or Human Resources. This role is ideal for someone looking to gain hands-on experience, build confidence, and actively contribute to real projects in a small but growing business environment.
  
  You’ll support a wide range of activities across sales, marketing, and HR—giving you a broad understanding of how each function operates in the real-world settings. While the role is unpaid, all travel-related expenses for client visits will be fully covered.Key Responsibilities
  • Handle inbound and outbound telephone calls in a professional manner.
  • Conduct cold calling to engage potential leads and introduce services.
  • Set up meetings and appointments with prospective clients.
  • Support social media content creation, scheduling, and engagement across platforms.
  • Assist with turning leads into potential customers through consistent follow-up.
  • Work towards converting every qualified lead into a customer—performance incentives provided.
  • Conduct market research and competitor analysis where required.
  • Assist with CRM updates, candidate data, or marketing performance tracking.
  • Help with outreach materials, reporting, and administrative tasks.
  • Join occasional client meetings (travel expenses reimbursed).
  
  
  RequirementsWhat We’re Looking For
  • A recent university leaver with a degree in Sales, Marketing & Management, or HR.
  • Enthusiastic, dedicated, and eager to learn quickly.
  • Confident handling phone calls and speaking with clients.
  • Comfortable with cold calling and initiating conversations.
  • Strong written and verbal communication skills.
  • Fully tuned into social media marketing (LinkedIn, Instagram, TikTok, etc.).
  • Organised, reliable, and able to manage tasks independently.
  • A positive, proactive attitude with an interest in gaining real-world experience.
  • Professional and comfortable interacting with clients.
  
  
  BenefitsWhat You’ll Gain
  • Hands-on experience in sales, marketing, and HR.
  • Confidence in handling calls, cold outreach, and client engagements.
  • Experience in lead generation and customer conversion.
  • Practical understanding of social media marketing.
  • Mentoring and guidance to support career development.
  • Performance-based incentives for conversions.
  • Travel expenses fully reimbursed for any client visits.
  How to Apply
  Please send your CV and a short introduction explaining why you’re interested in this opportunity.
  
  
  
  Requirements
  What We’re Looking For • A recent university leaver with a degree in Sales, Marketing & Management, or HR. • Enthusiastic, dedicated, and eager to learn quickly. • Confident handling phone calls and speaking with clients. • Comfortable with cold calling and initiating conversations. • Strong written and verbal communication skills. • Fully tuned into social media marketing (LinkedIn, Instagram, TikTok, etc.). • Organised, reliable, and able to manage tasks independently. • A positive, proactive attitude with an interest in gaining real-world experience. • Professional and comfortable interacting with clients. Read Less

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• 

  Clinical Research Coordinator  

  MastarRec

  [fulltime] - Manchester

  Posted: 01/12/2025

  Apply Now

  Job DescriptionJob DescriptionWe are seeking detail-oriented Clinical... Read More

  Job Description
  Job Description
  We are seeking detail-oriented Clinical Research Coordinator (CRC) to oversee and manage clinical trial activities, ensuring strict adherence to GCP guidelines, regulatory requirements, and study protocols. You will play a critical role in coordinating all aspects of clinical research — from participant recruitment to data management and compliance monitoring — to support the delivery of groundbreaking medical advancements.
  This is an exciting opportunity to work at the intersection. Of healthcare innovation, patient care, and research excellence in a collaborative, fast-paced environment.
  
  Job Responsibilities
  Coordinate and manage the day-to-day operations of clinical studies
  Recruit, screen, and consent eligible study participants in accordance with IRB-approved protocols
  Maintain accurate and up-to-date source documentation and electronic data capture (EDC) systems
  Monitor patient safety, schedule study visits, and ensure protocol adherence
  Liaise with principal investigators, sponsors, and ethics committees
  Prepare regulatory documentation, site initiation, and close-out reports
  Track study progress and submit timely updates to stakeholders
  Ensure quality assurance and compliance with ICH-GCP, MHRA, and institutional regulations
  
  
  RequirementsRequired Skills
  In-depth knowledge of GCP, clinical research regulations, and ethical standards
  Experience with clinical data collection, source documentation, and informed consent processes
  Proficiency with electronic data capture systems (e.g., REDCap, Medidata, or similar)
  Strong organizational and time management skills
  Excellent communication and interpersonal abilities
  Detail-oriented and able to handle multiple trials simultaneously
  
  Desired Skills
  Bachelor’s degree in Life Sciences, Nursing, or Health Sciences
  ACRP or SOCRA certification
  Previous experience in oncology, cardiology, or rare disease clinical trials
  Familiarity with clinical trial software platforms and regulatory submissions
  
  
  BenefitsJob Benefits
  Competitive salary with annual performance bonuses
  Training and career development in clinical operations and trial management
  Private health insurance and pension plan
  Supportive work environment with flexible working options
  Work with a cross-disciplinary team of clinical and research experts
  
  
  
  Requirements
  Required Skills Strong knowledge of PCR, ELISA, Western blotting Data recording and lab documentation skills BSc or MSc in Molecular Biology/Biotech Desired Skills CRISPR or RNA-based tech exposure GLP/GMP environment familiarity Read Less

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