Assistant Clinical Research Associate

Assistant Clinical Research Associate

Client:

Thermo Fisher Scientific

Location:

Austria

Job Category:

Other

EU work permit required:

Yes

Job Reference:

2cca6535a7a0

Job Views:

3

Posted:

24.03.2025

Expiry Date:

08.05.2025

Job Description:

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.

Summarized Purpose:

Performs remote activities on assigned projects in liaison with the Remote CRA, On-Site CRA and study CTM. Provides support with regards to site preparedness, logistical support to the monitoring process, and assists with assigned tasks for site management and remote monitoring in accordance with SOPs and regulatory guidelines.

Key responsibilities:

• Completes study and site management activities as defined in task matrix.
• Completes and documents study-specific training.
• Orients and trains on any CRG/study-specific systems.
• Provides in-house support during pre-study assessments.
• Supports customization of Site ICF with site contact details, as needed.
• Performs remote review of EMR/EHR checklist and supports collection as applicable.
• Verifies document collection and RCR submission status.
• Reviews patient-facing materials and translations, as directed.
• Supports site staff with the vendor-related qualification process.
• Ensures system access is requested/granted and revoked for relevant site staff.
• Follows up on site staff training, as applicable.
• Coordinates and supports logistics for IM attendance.
• Maintains vendor trackers.
• Coordinates study/site supply management.
• Supports crucial document collection, review, and updating in systems.
• Follows up on missing study vendor data.
• Supports ongoing remote review of centralized monitoring tools.
• Coordinates site payments processes.
• Performs reconciliation tasks on assigned trials.
• Verifies document collection status in CRG systems.
• May perform other assigned site management tasks.
• Maintains administrative tasks such as expense reports and timesheets.

Keys to Success:

Education and Experience:

Bachelor's degree or equivalent and relevant formal academic/vocational qualification. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).

Knowledge, Skills and Abilities:

• Basic medical/therapeutic area knowledge and understanding of medical terminology.
• Ability to attain and maintain a solid understanding of ICH GCP, applicable regulations, and CRG procedural documents.
• Effective oral and written communication skills.
• Excellent interpersonal and customer service skills.
• Good interpersonal and time management skills with strong attention to detail.
• Proven flexibility and adaptability.
• Ability to work in a team or independently.
• Well-developed critical thinking skills.
• Proficient digital literacy with good knowledge of MS Office.
• Ability to extract pertinent information from study documents and electronic systems.
• Excellent English language and grammar skills.

We offer competitive remuneration, an annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects.