CrawlJobs Logo

Research Associate

United Kingdom, Warrington 37694.00 - 46049.00 GBP / Year · Job Posted June 01, 2026
Apply Position
Job Link Share

Job Description

We are seeking a motivated and collaborative individual to join our team as a Research Associate. This role offers an exciting opportunity to contribute to a translational research project focused on developing a mammalian-produced, bioactive BMP13 (GDF6) reagent for intervertebral disc and cartilage repair. You will work at the interface of regenerative medicine, protein science and industry collaboration within a dynamic and inclusive environment.

Job Responsibility

  • Designing and delivering experimental studies to support development of bioactive BMP13 for regenerative medicine applications
  • Optimising mammalian expression systems, construct design and protein processing to enhance yield and activity
  • Conducting protein analysis and bioactivity testing using biochemical and functional assays
  • Analysing and interpreting experimental data, maintaining accurate records and contributing to reproducible research practices
  • Collaborating with academic and industrial partners and contributing to reports, publications and dissemination activities

Requirements

  • A PhD (or near completion) in a relevant discipline such as biochemistry, molecular biology, biotechnology or regenerative medicine
  • Hands-on experience in mammalian cell culture and molecular biology techniques (e.g. cloning, construct design)
  • Experience with protein analysis methods (e.g. SDS-PAGE, Western blotting, ELISA)
  • Strong data analysis, organisational and problem-solving skills, with the ability to manage complex experimental workflows
  • Excellent communication skills and ability to work independently and collaboratively in a multidisciplinary environment

Nice to have

  • Experience in mammalian expression optimisation or protein purification and downstream processing
  • Familiarity with advanced analytical or biophysical techniques (e.g. HPLC, mass spectrometry)
  • Experience working on translational or industry-linked research projects
  • Experience contributing to publications, funding applications or collaborative research outputs
  • Experience supporting or mentoring students or junior colleagues

What we offer

  • Generous employer contribution pension
  • 29 days annual leave plus bank holidays, along with Christmas closure
  • Ride to work and EV car scheme available

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

Research Associate

8 matching positions

Clinical Research Associate II/Sr. Clinical Research Associate - Oncology

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
United States
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
  • Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
  • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
  • Must be fluent in English and in the native language(s) of the country they will work in
  • Ability to travel 60-80%
  • Valid driver’s license and passport required
  • Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
Job Responsibility
Job Responsibility
  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and the Sponsor's standards to achieve project goals, timelines and quality
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
  • Serve as the primary point of contact for assigned investigator sites
  • Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
  • Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
  • Provide protocol training to, and address protocol related questions from the investigator site staff when required
  • Attend investigator meeting when required (virtual or F2F)
  • Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators
  • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities
  • Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed
What we offer
What we offer
  • Flexible work arrangements
  • Career growth and development
  • Supportive and inclusive environment
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
Read More
Arrow Right

Digital research associate / assistant

RONIN International is an independent, multi-award winning market research and c...
Location
Location
Germany , Hamburg
Salary
Salary:
Not provided
ronin.com Logo
RONIN International
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Think logically and creatively
  • Always open-minded and interested in exploring new solutions and new tools
  • Work extremely precisely and meticulously
  • Have excellent written communication skills
  • Interaction with senior participants is matter-of-fact and confident
  • Confident in communicating with participants in other countries and with different cultural backgrounds
  • Can organize your work well
  • Have no difficulty working under pressure or with tight schedules
  • Can deliver high-quality results independently
  • Can work on multiple projects at the same time
Job Responsibility
Job Responsibility
  • Gain a deep understanding of the requirements and relevant profiles of each research project
  • Determine the digital approaches that are most suitable for the respective research project
  • Use different research methods to identify suitable potential participants for different projects
  • Recruit suitable participants for the research project
  • Manage campaigns on various social media platforms
  • Ensure that the individual steps mesh smoothly throughout the entire life cycle of a project
  • Coordinate regularly with other departments and other members within the Digital Department
  • Maintain complete records of the work progress of each project
  • Regularly report the progress of the projects assigned to you to Digital Supervisors and Digital Managers
  • Ensure that the requirements for efficiency and effectiveness are met for every project
  • Fulltime
Read More
Arrow Right

Soybean Research Associate

The soybean research associate will perform a variety of tasks associated with d...
Location
Location
United States , Horace
Salary
Salary:
Not provided
stineseed.com Logo
Stine Seed Company
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • You are a self-starter with systematic decision making, problem solving and troubleshooting skills and the ability to work independently
  • An interest in agronomic research
  • You have a High School diploma/GED, Associate of Applied Science, Associate of Science, B.S., or Bachelor’s degree in agronomy
  • You have strong written and verbal communication skills
  • You have a valid driver's license
  • may be required to obtain a Commercial Driver’s License (CDL)
  • Willing and able to work in a variety of areas, field, warehouse, office
  • Willing and able to stand and sit for extended periods
  • Willing and able to work both outdoors and indoors
  • Willing and able to perform physical work that involves repetitive motion and/or repetitive lifting including lifting to 50 pounds
Job Responsibility
Job Responsibility
  • Communicate effectively verbally and in writing with other team members
  • Preparation, sorting, cleaning, automated packaging, scanning, labeling, planting, and harvesting of seed for plots and nurseries
  • Willing/able to learn, operate and maintain basic farm equipment
  • including plot planters, sprayers, plot combines and small threshers
  • Willing to coordinate plot locations, measure and set flags
  • Ability to observe and collect plant data notes
  • Willing to learn hand pollination and harvesting in nursery
  • Willing and able to work routine weekends during peak seasons. Including travel to other states
  • Warehousing activities may include forklift operation
  • Various other duties as assigned
What we offer
What we offer
  • health/dental/vision insurance
  • retirement packages
  • Fulltime
Read More
Arrow Right

Soybean Research Associate

This is an excellent opportunity to grow with one of the industry’s most respect...
Location
Location
United States , Adel
Salary
Salary:
Not provided
stineseed.com Logo
Stine Seed Company
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • You are a self-starter with systematic decision making, problem solving and troubleshooting skills and the ability to work independently
  • An interest in agronomic research
  • You have a High School diploma/GED, Associate of Applied Science, Associate of Science, B.S., or Bachelor’s degree in agronomy
  • You have strong written and verbal communication skills
  • You have a valid driver's license
  • may be required to obtain a Commercial Driver’s License (CDL)
  • Willing and able to work in a variety of areas, field, warehouse, office
  • Willing and able to stand and sit for extended periods
  • Willing and able to work both outdoors and indoors
  • Willing and able to perform physical work that involves repetitive motion and/or repetitive lifting including lifting to 50 pounds
Job Responsibility
Job Responsibility
  • Communicate effectively verbally and in writing with other team members
  • Preparation, sorting, cleaning, automated packaging, scanning, labeling, planting, and harvesting of seed for plots and nurseries
  • Willing/able to learn, operate and maintain basic farm equipment
  • including plot planters, sprayers, plot combines and small threshers
  • Willing to coordinate plot locations, measure and set flags
  • Ability to observe and collect plant data notes
  • Willing to learn hand pollination and harvesting in nursery
  • Willing and able to work routine weekends during peak seasons, including travel to other states
  • Warehousing activities may include forklift operation
  • Various other duties as assigned
What we offer
What we offer
  • health/dental/vision insurance
  • retirement packages
  • Fulltime
Read More
Arrow Right

Corn Research Associate

Stine Seed Company, the nation’s largest independent seed company, is seeking ta...
Location
Location
United States , Adel
Salary
Salary:
Not provided
stineseed.com Logo
Stine Seed Company
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • You are a strong team member, self-starter with systematic decision making, problem solving and troubleshooting skills with the ability to work independently
  • You have an interest in agronomic research
  • You have a High School diploma/GED, Associate of Applied Science, Associate of Science, B.S., or Bachelor’s degree in agronomy
  • You must possess a valid driver's license and may be required to obtain a Commercial Driver’s License (CDL) in the future
  • Willing and able to work in a variety of areas, (field, warehouse, and office)
  • Willing and able to stand and sit for extended periods
  • Willing and able to work both outdoors and indoors in hot, cold, wet, and dry conditions
  • Willing and able to lift to 50 lbs. and complete work that involves repetitive motion and/or repetitive lifting
  • Willing and able to work overtime hours including weekend work required during seasonal peaks. This includes overnight trips to off-site locations and additional travel as necessary at off-site locations
  • You have strong interpersonal, written, and verbal communication skills
Job Responsibility
Job Responsibility
  • Communicate effectively verbally and in writing with team members and crew leaders
  • Preparation, sorting, cleaning, automated packaging, and labeling of seed for plots and nurseries
  • Knowledge/willing to learn operation and maintenance of a corn plot planter
  • Knowledge/willing to learn operation of a corn combine for yield trial data
  • Willing and able to spray crops, maintain sprayer and equipment
  • Willing to apply or have pesticide applicator certification
  • Willing and able to observe and collect plant data notes
  • Willing to learn hand pollination and harvesting in nursery
  • Willing and able to work routine weekends during peak seasons. Peak season is seven days per week and includes travel to other states during summer months
  • Ability to work in an organized and safe manner independently
What we offer
What we offer
  • health/dental/vision insurance
  • retirement packages
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
Taiwan , Taipei
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree in a relevant field such as life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Job Responsibility
Job Responsibility
  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
Read More
Arrow Right

Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
China , Chengdu
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills, with attention to detail
  • Ability to work independently and collaboratively in a fast-paced environment
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Job Responsibility
Job Responsibility
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
  • Collaborating with investigators and site staff to facilitate smooth study conduct
  • Performing data review and resolution of queries to maintain high-quality clinical data
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Fulltime
Read More
Arrow Right

Clinical Research Associate II

Clinical Research Associate - Remote - FSP. ICON plc is a world-leading healthca...
Location
Location
Greece , Athens
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills, with attention to detail
  • Ability to work independently and collaboratively in a fast-paced environment
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Job Responsibility
Job Responsibility
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
  • Collaborating with investigators and site staff to facilitate smooth study conduct
  • Performing data review and resolution of queries to maintain high-quality clinical data
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Fulltime
Read More
Arrow Right