Study Nurse

Apsida Life Science; Tirol; On-site; EUR 32,000 - 52,000; Part time

Job summary

Apsida Life Science seeks a Study Nurse to support GI studies at our Hall in Tirol site. This on-site, part-time/contract role includes coordinating study activities, data entry into eCRF systems, venipuncture, and patient follow-up. Start ASAP with onboarding by Oct 2026 and end date in June 2028.

Requirements include at least 2 years in clinical research, active GCP/IATA/BLS certifications, and willingness to travel to Hall in Tirol (about 1.5 hours one-way). The position is on-site in Austria.

Qualifications

• Minimum of 2 years of clinical research experience.
• Active GCP, IATA, and BLS certifications are required.
• Willingness to travel to Hall in Tirol (approx. 1.5 hours travel time).

Responsibilities

• Support study coordination and assist the site team with overall study organization.
• Enter clinical data accurately into eCRF systems in a timely manner.
• Support Clinical Protocol activities as capacity allows.
• Perform venipuncture and basic lab processing.
• Measure and record vital signs.
• Follow up with patients and track study-related activities.

Skills

Clinical research

Study coordination

Venipuncture

Vital signs

Data entry

Patient follow-up

Tools

eCRF systems

Lab processing

Job description

Job Title: Study Nurse (Gastro-Intestinal Study)

Location: Hall in Tirol, Austria (On-site)

Type: Contract / Freelance / Part-Time

Start Date: ASAP (Onboarding by end of October 2026)

End Date: June 2028

Company Overview:

Apsida Life Science is partnering with an international clinical research services provider that supports the delivery of clinical trials through specialised site-level expertise and patient-focused services. The organisation collaborates with pharmaceutical and biotechnology companies to facilitate study coordination, clinical assessments, patient monitoring and data management.

Key Responsibilities:

• Study Coordination Support: Assisting the site team with overall study organization.
• Data Entry: Timely and accurate entry of clinical data into eCRF systems.
• Clinical Protocol Support (depending on site capacity):
• Venipuncture / Blood draws and lab processing
• Measuring and recording vital signs
• Patient follow-up and tracking

Requirements & Qualifications:

• Experience: Minimum of 2 years of clinical research experience.
• Certifications: Active GCP, IATA, and BLS certifications are required.
• Location & Travel: Willingness to travel to Hall in Tirol (approx. 1.5 hours one-way travel time).