Posted by ZMed is hiring a Clinical Trials Data Entry Specialist to support the management and development of clinical studies at its center in Las Palmas de Gran Canaria, Spain. This is a full-time, on-site position within the company’s clinical trials coordination team.
The successful candidate will work closely with researchers, clinical trial coordinators, monitors, and sponsors to support the accurate management of clinical study information. The role includes entering and updating clinical data, managing study documentation, following up on data queries, and assisting with different stages of clinical trials.
Job Overview
- Job Title: Clinical Trials Data Entry Specialist
- Company: ZMed
- Location: Las Palmas de Gran Canaria, Las Palmas province, Spain
- Employment Type: Full-time
- Work Arrangement: On-site
- Job Field: Clinical research and clinical trial data management
- Education: Training related to healthcare or a scientific field
- Experience: Experience in clinical trials, clinical research, or data management is valued
- Clinical Trial Systems: Knowledge of clinical trial management platforms and CRD/eCRF is valued
- English: English proficiency is valued, particularly for international study documentation and platforms
About the Employer
ZMed is recruiting a new member for its clinical trials coordination team in Las Palmas de Gran Canaria. The selected candidate will collaborate with investigators, coordinators, monitors, and sponsors to support the proper management of clinical studies.
Job Description
The Clinical Trials Data Entry Specialist will support the accurate recording, updating, and management of clinical study data. The position involves entering clinical information into CRD/eCRF systems and other sponsor platforms while following established study protocols and procedures.
The role also involves organizing clinical trial and patient documentation, addressing data queries, assisting with monitoring activities, and supporting the coordination team throughout different stages of clinical studies.
Key Responsibilities
The successful candidate will be responsible for:
- Entering and updating clinical data in CRD/eCRF systems and other sponsor platforms.
- Reviewing submitted information and following up on queries related to clinical data.
- Preparing, organizing, and maintaining clinical study and patient documentation.
- Supporting the clinical trials coordination team with study management and follow-up activities.
- Preparing documents and information required for monitoring visits.
- Supporting study initiation, follow-up, and close-out visits.
- Working with investigators, coordinators, and monitors to ensure study information remains properly updated.
- Filing and maintaining documentation related to clinical trials.
- Carrying out other support duties associated with the clinical research team.
Qualifications and Requirements
Candidates should have an educational background related to the healthcare or scientific field.
The employer also values the following:
- Previous experience in clinical trials.
- Experience in clinical research.
- Experience in data management.
- Strong organizational skills.
- Good attention to detail.
- Ability to work effectively as part of a team.
- Knowledge of clinical trial management platforms.
- Familiarity with CRD/eCRF systems.
- English language skills, particularly for managing documentation and platforms used in international studies.
The listing presents experience in clinical trials, clinical research, or data management, as well as knowledge of clinical trial platforms and English proficiency, as valued qualifications.
Salary and Benefits
The job listing does not provide information about the salary or specific employee benefits.
The position is offered on a full-time basis and requires the successful candidate to work on-site in Las Palmas de Gran Canaria.
Who Should Apply?
This position may suit candidates with a healthcare or scientific educational background who are interested in clinical research and clinical trial data management.
Candidates with experience in clinical trials, clinical research, or data management may be well suited to the responsibilities of the role. Strong organizational skills, attention to detail, teamwork, and familiarity with clinical trial data systems are also valued.
Frequently Asked Questions
What is the job title?
The position is for a Clinical Trials Data Entry Specialist.
Where is the Clinical Trials Data Entry Specialist job located?
The position is located in Las Palmas de Gran Canaria, Las Palmas province, Spain.
Is this a full-time position?
Yes. The job is advertised as a full-time position.
Is the position remote?
No. The listing states that the position is on-site.
What educational background is required?
Candidates should have training related to a healthcare or scientific field.
Is previous clinical trial experience required?
Experience in clinical trials, clinical research, or data management is valued, although the listing does not state that previous experience is mandatory.
Is knowledge of CRD/eCRF required?
Knowledge of clinical trial management platforms and CRD/eCRF is valued for the position.
Does the job offer visa sponsorship or accommodation?
The provided job listing does not mention visa sponsorship, relocation assistance, or accommodation.
How to Apply
Interested candidates who meet the required qualifications and experience criteria should submit their application.
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