1,854 Biomedical Research jobs in the United Kingdom
Senior Biomedical Research Scientist - Genomics
SO14 0AA Southampton, South East
£60000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Join our leading scientific research organisation as a Senior Biomedical Research Scientist, focusing on cutting-edge genomics and molecular biology. This is a fully remote position, allowing you to contribute to groundbreaking discoveries from anywhere in the UK. You will play a pivotal role in designing and executing complex research projects aimed at understanding genetic underpinnings of diseases and developing novel therapeutic strategies. Your expertise will be crucial in analysing large-scale genomic datasets, validating findings, and contributing to high-impact publications. This role requires a deep understanding of molecular biology techniques, bioinformatics, and a passion for pushing the boundaries of biomedical science.
Key Responsibilities:
Key Responsibilities:
- Lead independent research projects in genomics and molecular biology, from experimental design to data interpretation.
- Develop and optimize high-throughput genomic assays and protocols.
- Analyse and interpret complex genomic datasets (e.g., WGS, WES, RNA-Seq) using advanced bioinformatics tools and pipelines.
- Collaborate with computational biologists and statisticians to integrate multi-omics data.
- Validate key findings using a range of molecular and cell biology techniques.
- Write and publish research findings in peer-reviewed journals and present at international conferences.
- Mentor and guide junior research staff and students.
- Contribute to grant writing and secure external funding.
- Stay current with the latest advancements in genomics, transcriptomics, and related fields.
- Ensure adherence to ethical guidelines and research integrity.
- Proactively identify new research opportunities and directions.
- Contribute to the overall scientific strategy of the research group.
- Ph.D. in Genetics, Molecular Biology, Biomedical Science, or a closely related field.
- Minimum of 5 years of post-doctoral research experience with a strong publication record in genomics or a related area.
- Demonstrated expertise in molecular biology techniques (PCR, qPCR, cloning, NGS library preparation, etc.).
- Proficiency in bioinformatics tools and scripting languages (e.g., R, Python) for genomic data analysis.
- Experience with public genomic databases and resources.
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively in a remote setting.
- Proven ability to manage multiple research projects simultaneously.
- Experience in mentoring junior scientists.
- A proactive and independent work ethic is essential for this remote role.
This advertiser has chosen not to accept applicants from your region.
0
Clinical Research Scientist
NG1 1 Nottingham, East Midlands
£55000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a pioneering pharmaceutical company, is seeking a highly skilled and motivated Clinical Research Scientist to join their innovative, fully remote research and development team. This crucial role will involve contributing to the design, execution, and analysis of clinical trials, with a focus on (Specific therapeutic area, e.g., oncology, immunology, rare diseases). You will be instrumental in advancing novel drug candidates through the development pipeline, from pre-clinical research to regulatory submission. The ideal candidate will possess a strong scientific background, meticulous attention to detail, and the ability to thrive in a fast-paced, virtual research environment. This is an exceptional opportunity to contribute to life-changing medical advancements from the comfort of your home.
Responsibilities:
Responsibilities:
- Contribute to the design and development of clinical trial protocols, ensuring scientific integrity and regulatory compliance.
- Oversee the execution of clinical trials, including site selection, investigator meetings, and monitoring activities.
- Analyze and interpret complex clinical data, preparing comprehensive reports and presentations for internal stakeholders and regulatory agencies.
- Collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and project management.
- Stay abreast of the latest scientific literature, emerging technologies, and regulatory guidelines relevant to clinical research.
- Contribute to the writing of investigational new drug (IND) applications, clinical study reports (CSRs), and manuscripts for publication.
- Identify and mitigate risks associated with clinical trial execution.
- Manage relationships with external collaborators, key opinion leaders (KOLs), and contract research organizations (CROs).
- Contribute to the development of scientific strategies and pipeline planning.
- Ensure all research activities are conducted in compliance with Good Clinical Practice (GCP) guidelines and company policies.
- Ph.D. or Master's degree in a relevant scientific discipline (e.g., life sciences, pharmacology, biomedical science).
- Minimum of 5 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry.
- Demonstrated experience in designing, conducting, and analyzing clinical trials.
- Strong understanding of drug development processes and regulatory requirements (e.g., FDA, EMA).
- Excellent scientific writing and data analysis skills.
- Proficiency in statistical software and data management systems is a plus.
- Exceptional communication, collaboration, and interpersonal skills.
- Ability to work independently, manage multiple projects simultaneously, and meet tight deadlines in a remote setting.
- Experience in (Specific therapeutic area) is highly desirable.
- Proven ability to critically evaluate scientific data and contribute to strategic decision-making.
- Must have a dedicated home office setup with reliable high-speed internet to perform duties effectively.
This advertiser has chosen not to accept applicants from your region.
1
Clinical Research Nurse
Cornwall, South West
EmVenio
Posted today
Job Viewed
Job Description
Make a Difference on Your Own Schedule and Terms! Summary The Certified Mobile Research Nurse is a Registered Nursing ad-hoc/PRN position for EmVenio Clinical Research. Our CMRN is responsible for setting appointments within the required visitation window to complete mobile visits for study participants. You’ll work cooperatively with Clinical Project Managers, Coordinators, and site personnel to complete visits and submit accurate source documentation. We are looking for RGNs with current venepuncture and physical assessment competency to conduct visits with adult patients in their homes. The ability to drive with access to your own vehicle is a mandatory requirement for this position. Required Qualifications Full NMC registration with a minimum of two (2) years of experience as a Registered Nurse (RN) and no restrictions on practice Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw and Port access for administering infusions (date of last practice within 6 months, preferred) One (1) year of experience conducting full head-to-toe physical assessments, including using a stethoscope One (1) year of experience collecting vital signs, ECG, urine samples, and performing urine pregnancy tests Clean DBS Skilled at collecting accurate, detailed patient records including documentation of medical history and medication charting Excellent observational, verbal, written communication, and problem-solving skills Must have and maintain a current CPR certification Must have and maintain a current vaccination record Full, clean driving license with access to own vehicle Personal Incentives Gain GCP training certification Be a member of our general staffing pool with access to multiple study opportunities No research experience required, on the job training provided Contribute to advancements of truly life changing treatments Supporting the same patient throughout the trial, being on the cutting-edge of developing new groundbreaking treatments for a disease with high unmet need
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Associate
London, London
Barrington James
Posted today
Job Viewed
Job Description
Job Title: Junior Clinical Research Associate (CRA) Location: London, UK (Field-based with regular site visits) Employment Type: Full-time About the Role: We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols. Key Responsibilities: Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions. Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements. Verify accuracy and completeness of case report forms (CRFs) against source data. Identify and resolve data discrepancies and protocol deviations in collaboration with site staff. Maintain effective communication with investigators, site personnel, and internal study teams. Prepare and submit timely monitoring reports and follow-up documentation. Support investigators and sites in resolving queries and ensuring readiness for audits and inspections. Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection). Requirements: Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field. Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment. Strong knowledge of ICH-GCP and UK clinical trial regulations. Excellent organizational and time management skills with the ability to manage multiple sites. Willingness to travel frequently (4–6 site visits per month). Strong interpersonal and communication skills, both written and verbal. What We Offer: Competitive salary and benefits package. Professional development opportunities within a growing clinical operations team. Exposure to diverse therapeutic areas and phases of clinical development. Supportive work environment with mentorship from senior CRAs.
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Associate
London, London
Barrington James
Posted today
Job Viewed
Job Description
Job Title: Junior Clinical Research Associate (CRA) Location: London, UK (Field-based with regular site visits) Employment Type: Full-time About the Role: We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols. Key Responsibilities: Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions. Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements. Verify accuracy and completeness of case report forms (CRFs) against source data. Identify and resolve data discrepancies and protocol deviations in collaboration with site staff. Maintain effective communication with investigators, site personnel, and internal study teams. Prepare and submit timely monitoring reports and follow-up documentation. Support investigators and sites in resolving queries and ensuring readiness for audits and inspections. Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection). Requirements: Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field. Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment. Strong knowledge of ICH-GCP and UK clinical trial regulations. Excellent organizational and time management skills with the ability to manage multiple sites. Willingness to travel frequently (4–6 site visits per month). Strong interpersonal and communication skills, both written and verbal. What We Offer: Competitive salary and benefits package. Professional development opportunities within a growing clinical operations team. Exposure to diverse therapeutic areas and phases of clinical development. Supportive work environment with mentorship from senior CRAs.
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Nurse
Plymouth, South West
EmVenio
Posted today
Job Viewed
Job Description
Make a Difference on Your Own Schedule and Terms! Summary The Certified Mobile Research Nurse is a Registered Nursing ad-hoc/PRN position for EmVenio Clinical Research. Our CMRN is responsible for setting appointments within the required visitation window to complete mobile visits for study participants. You’ll work cooperatively with Clinical Project Managers, Coordinators, and site personnel to complete visits and submit accurate source documentation. We are looking for RGNs with current venepuncture and physical assessment competency to conduct visits with adult patients in their homes. The ability to drive with access to your own vehicle is a mandatory requirement for this position. Required Qualifications Full NMC registration with a minimum of two (2) years of experience as a Registered Nurse (RN) and no restrictions on practice Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw and Port access for administering infusions (date of last practice within 6 months, preferred) One (1) year of experience conducting full head-to-toe physical assessments, including using a stethoscope One (1) year of experience collecting vital signs, ECG, urine samples, and performing urine pregnancy tests Clean DBS Skilled at collecting accurate, detailed patient records including documentation of medical history and medication charting Excellent observational, verbal, written communication, and problem-solving skills Must have and maintain a current CPR certification Must have and maintain a current vaccination record Full, clean driving license with access to own vehicle Personal Incentives Gain GCP training certification Be a member of our general staffing pool with access to multiple study opportunities No research experience required, on the job training provided Contribute to advancements of truly life changing treatments Supporting the same patient throughout the trial, being on the cutting-edge of developing new groundbreaking treatments for a disease with high unmet need
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Nurse
Bristol, South West
EmVenio
Posted today
Job Viewed
Job Description
Make a Difference on Your Own Schedule and Terms! Summary The Certified Mobile Research Nurse is a Registered Nursing ad-hoc/PRN position for EmVenio Clinical Research. Our CMRN is responsible for setting appointments within the required visitation window to complete mobile visits for study participants. You’ll work cooperatively with Clinical Project Managers, Coordinators, and site personnel to complete visits and submit accurate source documentation. We are looking for RGNs with current venepuncture and physical assessment competency to conduct visits with adult patients in their homes. The ability to drive with access to your own vehicle is a mandatory requirement for this position. Required Qualifications Full NMC registration with a minimum of two (2) years of experience as a Registered Nurse (RN) and no restrictions on practice Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw and Port access for administering infusions (date of last practice within 6 months, preferred) One (1) year of experience conducting full head-to-toe physical assessments, including using a stethoscope One (1) year of experience collecting vital signs, ECG, urine samples, and performing urine pregnancy tests Clean DBS Skilled at collecting accurate, detailed patient records including documentation of medical history and medication charting Excellent observational, verbal, written communication, and problem-solving skills Must have and maintain a current CPR certification Must have and maintain a current vaccination record Full, clean driving license with access to own vehicle Personal Incentives Gain GCP training certification Be a member of our general staffing pool with access to multiple study opportunities No research experience required, on the job training provided Contribute to advancements of truly life changing treatments Supporting the same patient throughout the trial, being on the cutting-edge of developing new groundbreaking treatments for a disease with high unmet need
This advertiser has chosen not to accept applicants from your region.
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6
Clinical Research Nurse
Southampton, South East
EmVenio
Posted today
Job Viewed
Job Description
Make a Difference on Your Own Schedule and Terms! Summary The Certified Mobile Research Nurse is a Registered Nursing ad-hoc/PRN position for EmVenio Clinical Research. Our CMRN is responsible for setting appointments within the required visitation window to complete mobile visits for study participants. You’ll work cooperatively with Clinical Project Managers, Coordinators, and site personnel to complete visits and submit accurate source documentation. We are looking for RGNs with current venepuncture and physical assessment competency to conduct visits with adult patients in their homes. The ability to drive with access to your own vehicle is a mandatory requirement for this position. Required Qualifications Full NMC registration with a minimum of two (2) years of experience as a Registered Nurse (RN) and no restrictions on practice Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw and Port access for administering infusions (date of last practice within 6 months, preferred) One (1) year of experience conducting full head-to-toe physical assessments, including using a stethoscope One (1) year of experience collecting vital signs, ECG, urine samples, and performing urine pregnancy tests Clean DBS Skilled at collecting accurate, detailed patient records including documentation of medical history and medication charting Excellent observational, verbal, written communication, and problem-solving skills Must have and maintain a current CPR certification Must have and maintain a current vaccination record Full, clean driving license with access to own vehicle Personal Incentives Gain GCP training certification Be a member of our general staffing pool with access to multiple study opportunities No research experience required, on the job training provided Contribute to advancements of truly life changing treatments Supporting the same patient throughout the trial, being on the cutting-edge of developing new groundbreaking treatments for a disease with high unmet need
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Associate
Barrington James
Posted 2 days ago
Job Viewed
Job Description
Job Title: Junior Clinical Research Associate (CRA)
Location: London, UK (Field-based with regular site visits)
Employment Type: Full-time
About the Role:
We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols.
Key Responsibilities:
- Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions.
- Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements.
- Verify accuracy and completeness of case report forms (CRFs) against source data.
- Identify and resolve data discrepancies and protocol deviations in collaboration with site staff.
- Maintain effective communication with investigators, site personnel, and internal study teams.
- Prepare and submit timely monitoring reports and follow-up documentation.
- Support investigators and sites in resolving queries and ensuring readiness for audits and inspections.
- Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection).
Requirements:
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
- Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment.
- Strong knowledge of ICH-GCP and UK clinical trial regulations.
- Excellent organizational and time management skills with the ability to manage multiple sites.
- Willingness to travel frequently (4–6 site visits per month).
- Strong interpersonal and communication skills, both written and verbal.
What We Offer:
- Competitive salary and benefits package.
- Professional development opportunities within a growing clinical operations team.
- Exposure to diverse therapeutic areas and phases of clinical development.
- Supportive work environment with mentorship from senior CRAs.
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Associate
London, London
Barrington James
Posted 2 days ago
Job Viewed
Job Description
Job Title: Junior Clinical Research Associate (CRA)
Location: London, UK (Field-based with regular site visits)
Employment Type: Full-time
About the Role:
We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols.
Key Responsibilities:
- Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions.
- Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements.
- Verify accuracy and completeness of case report forms (CRFs) against source data.
- Identify and resolve data discrepancies and protocol deviations in collaboration with site staff.
- Maintain effective communication with investigators, site personnel, and internal study teams.
- Prepare and submit timely monitoring reports and follow-up documentation.
- Support investigators and sites in resolving queries and ensuring readiness for audits and inspections.
- Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection).
Requirements:
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
- Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment.
- Strong knowledge of ICH-GCP and UK clinical trial regulations.
- Excellent organizational and time management skills with the ability to manage multiple sites.
- Willingness to travel frequently (4–6 site visits per month).
- Strong interpersonal and communication skills, both written and verbal.
What We Offer:
- Competitive salary and benefits package.
- Professional development opportunities within a growing clinical operations team.
- Exposure to diverse therapeutic areas and phases of clinical development.
- Supportive work environment with mentorship from senior CRAs.
This advertiser has chosen not to accept applicants from your region.
9