CRA Job Opportunity at Novotech | Apply Now
CRA job opportunities are highly sought-after in the global clinical research industry, and this role at Novotech offers an excellent entry point for freshers and early-career professionals. If you are looking to build a career in clinical research, life science job roles, or explore Spain jobs in biotech, this position provides hands-on exposure to clinical trials, regulatory processes, and global healthcare advancements.
- Job Position: Inhouse Clinical Research Associate (IHCRA)
- Location: Spain
About the Company
CRA job seekers exploring novotech careers will find Novotech to be a globally recognized full-service clinical Contract Research Organization (CRO).
Novotech is a global CRO specializing in clinical research and scientific advisory services. Founded in 1997, the company has expanded to 30+ offices across Asia-Pacific, the United States, and Europe. Known for its strong workplace culture and employee-focused programs, Novotech offers flexibility, professional development, and global career growth opportunities in the life science job sector.
Job Description
CRA job roles like this Inhouse Clinical Research Associate position provide in-house support to the clinical team according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Client SOPs.
The Inhouse Clinical Research Associate (IHCRA) provides in-house support to the clinical team according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Client SOPs.
Qualifications
- CRA job requirements for this Spain jobs opportunity include relevant education and early-career experience in clinical research or healthcare.
- Relevant experience/qualifications in Life Sciences or related field or administration would be preferable.
- Experience working in the pharmaceutical, CRO or healthcare industry is advantageous.
- Entry to less than 2 years’ experience as inhouse CRA or relevant roles.
Key Responsibilities
CRA job responsibilities in this life science job include supporting clinical operations and ensuring compliance with global standards.
- Support the clinical team’s inhouse activities on assigned projects
- Co-ordinate and maintain clinical study documentation in the Trial Master Files (TMF), including document tracking, audit preparation, QC reviews, and final reconciliation
- Support essential document development, collection, and management, including translations as per ICH GCP and SOPs
- Manage the Clinical Trial Management System (CTMS) and maintain accurate site compliance, milestones, and subject tracking
- Create Investigator Site Files and coordinate ordering, dispatch, and tracking of trial materials
- Ensure safe storage of study materials and maintain stock reports
- Assist CRAs with preparation for onsite or remote monitoring visits and follow-up actions
- Support IRB submissions, safety reporting (SUSAR, DSUR), and tracker management
- Assist with Clinical Trial Agreement (CTA) preparation, amendments, and budget negotiations
- Prepare and update Subject Visit Templates (SVTs) based on site budgets
- Manage Investigator payments tracking and support finance reconciliation activities
- Assist with vendor management, tracking, payments, and logistics including shipment and customs clearance
- Communicate with site staff/Investigators to resolve issues or request information
- Handle document archiving as per SOPs
- Track and report study safety events (SUSARs/CIOMS) to stakeholders
- Participate in Clinical Operations activities and contribute to SOP and process development
- Maintain professional communication representing the company positively
- Ensure adherence to company policies and maintain quality standards in all tasks
