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Medical Terminology jobs in West Midlands Region

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    • In this role, you'll ensure data quality and regulatory compliance while contributing to meaningful clinical research that improves health outcomes.
    • View all Thermo Fisher Scientific jobs - Birmingham jobs - Compliance Officer jobs in Birmingham
    • Salary Search: Data Compliance Coordinator salaries in Birmingham
    • This will include highly sensitive and complex medical terminology with a need for confidentiality.
    • Interpret clinical notes and phraseology of a continually…
    • The post holder will undertake a wide range of secretarial and administrative duties which includes digital audio transcription of complex clinical letters,…
    • Knowledge of medical terminology is preferred but not required.
    • Needs to have Medical Receptionist experience - *Hours of work are approx.
    • Strong knowledge of physiology, anatomy, and medical terminology.
    • Operate medical equipment safely and efficiently during procedures.
    • Full time, 37.5 hours/ week.
    • Monday to Friday, 08:00 – 16:00 or 09:00 – 17:00 (Flexibility on shift timings is required to cover out of hours MDT meetings).
  • View similar jobs with this employer
    • Strong knowledge of anatomy, physiology, and medical terminology.
    • Maintain accurate medical records and documentation.
    • Develop and implement nursing care plans.
    • Experience with medical documentation, medical records management, and medical terminology relevant to dentistry.
    • Pay: £450.00-£500.00 per day.
    • Familiarity with medical terminology relevant to speech-language pathology.
    • Contract: 5 hours per week across* our 3 complex nursing homes - Royal Park (WV2 2BL…
  • View similar jobs with this employer
    • Strong knowledge of anatomy, physiology, and medical terminology.
    • Maintain accurate medical records and documentation.
    • Develop and implement nursing care plans.
    • Field service experience with laboratory, medical or technical equipment.
    • £40,000-£46,000 | Company Vehicle Provided | Field‑Based Laboratory Role | Full…
    • Strong understanding of human anatomy, physiology, pathology, and medical terminology relevant to physiotherapy practice.
    • Knowledge of dental terminology and procedures.
    • Maintain organized filing systems for medical records and documentation review.
    • This is an excellent opportunity for an experienced medical administrator or secretary with strong knowledge of medical terminology, clinical systems and GP…

Job Post Details

Data Compliance Coordinator - job post

Thermo Fisher Scientific
3.4 out of 5 stars
Birmingham B15 2SQ
Full-time
You must create an Indeed account before continuing to the company website to apply

Job details

Job type

  • Full-time

Shift and schedule

  • Monday to Friday

Location

Birmingham B15 2SQ

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
Join our team at Thermo Fisher Scientific as a Corporate Compliance Associate II supporting clinical trials across our research sites. In this role, you'll ensure data quality and regulatory compliance while contributing to meaningful clinical research that improves health outcomes. You'll coordinate operational compliance activities across multiple studies, maintain critical documentation, and work closely with monitors and sponsor representatives to uphold the highest standards of data integrity. As part of our clinical research portfolio, you'll play an essential role in optimizing participant experiences in clinical trials and enabling life-changing therapies to reach those who need them.

REQUIREMENTS:
  • Minimum 1 year of relevant experience in clinical research, data management, or related field
  • Technical certification may be required for certain positions
  • Strong knowledge of ICH/GCP guidelines and regulatory requirements
  • Proficient in electronic Case Report Form (eCRF) data entry and query resolution
  • Experience maintaining Investigator Site Files (ISF) and study documentation
  • Excellent attention to detail and quality control capabilities
  • Strong time management skills with ability to handle multiple studies simultaneously
  • Proficiency in Microsoft Office applications
  • Ability to learn and apply medical terminology
  • Strong verbal and written communication skills in English
  • Bilingual skills may be required for specific positions
  • Ability to work both independently and collaboratively in a team environment
  • Experience with monitoring visit preparation and follow-up
  • Knowledge of data protection regulations and compliance requirements
  • Physical ability to be stationary for extended periods and perform computer work
  • Ability to travel occasionally as needed

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