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- Tasks: Monitor clinical trials and ensure compliance with protocols and regulations.
- Company: Join a leading clinical research organisation with a global impact.
- Benefits: Flexible freelance role with competitive pay and the chance to work remotely.
- Why this job: Make a difference in healthcare while utilising your language skills.
- Qualifications: 5+ years as a Clinical Research Associate and fluent in Serbian and English.
- Other info: Dynamic work environment with opportunities for professional growth.
The predicted salary is between 50000 - 60000 £ per year.
We have an immediate need for a FREELANCE Serbian Speaking & English Speaking SrCRA to join us. The Senior Clinical Research Associate position is responsible for clinical monitoring for assigned protocols and investigational sites. The role is responsible for ensuring that studies are conducted and documented in accordance with the study protocol, standard operating procedures, Good Clinical Practices (GCP) and other applicable regulatory requirements.
Main Responsibilities:
- Responsible for conduct of all types of monitoring, and co-monitoring visits and associated monitoring activities for assigned clinical sites both in person, and remote. This includes evaluation, site initiation, interim and close out monitoring visits.
- Responsible for monitoring report writing and completion within required SOP and local regulatory parameters.
- Support development of study specific documentation related to monitoring activities as assigned. This includes but is not limited to monitoring trackers, clinical monitoring guidelines, clinical monitoring plan, source document templates, site tools, and worksheets, etc.
- Responsible for site personnel management and training on the protocol requirements, proper source documentation procedures compliance, and case report completion requirements.
- Monitor assigned clinical trials and clinical sites by reviewing and reporting site enrollment, and termination updates, monitoring visits, protocol deviations, serious adverse events, laboratory abnormalities and any other activity at the site that contributes to proper conduct of the clinical trial per protocol, and regulatory requirements.
Necessary Skills and Abilities:
- Excellent verbal, written communication skills and interpersonal and presentation skills are required.
- Excellent computer skills with experience using Microsoft Office (Outlook, Word, Excel, and Power Point) applications to prepare charts, tables, forms, reports, and presentations required.
- Electronic data capture (EDC), CTMS, IVRS, and eTMF experience required.
- Knowledge of applicable local law, local regulatory requirements and regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials.
- Must be able to prioritize tasks, plan proactively, and accomplish goals using well-defined instructions and procedures with minimal supervision.
- Strong organizational skills and attention to details required.
- Ability to prioritize and plan workload is essential.
Educational Requirements:
- Bachelor's degree or equivalent combination of education and experience.
Experience Requirements:
- > 5 years of experience as a Clinical Research Associate.
Freelance Senior Clinical Research Associate - Serbian Speaking - up to 1 FTE in London employer: ProPharma Group
Contact Detail:
ProPharma Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Freelance Senior Clinical Research Associate - Serbian Speaking - up to 1 FTE in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who speak Serbian. They might know of opportunities that aren't advertised yet. Plus, a personal recommendation can go a long way!
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GCP and local regulations. Be ready to discuss how you've handled monitoring visits and site management in the past. We want to see your expertise shine!
✨Tip Number 3
Showcase your skills with a strong online presence. Update your LinkedIn profile to highlight your experience as a Senior Clinical Research Associate. Don’t forget to mention your language skills – being bilingual is a huge plus!
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect with us directly.
We think you need these skills to ace Freelance Senior Clinical Research Associate - Serbian Speaking - up to 1 FTE in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience as a Clinical Research Associate. We want to see how your skills align with the responsibilities mentioned in the job description, so don’t hold back on showcasing your expertise!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for this freelance role. We love seeing your personality come through, so feel free to share your passion for clinical research and any unique experiences that set you apart.
Showcase Your Language Skills: Since we’re looking for Serbian and English speakers, make sure to highlight your language proficiency clearly. Whether it’s in your CV or cover letter, let us know how fluent you are and any relevant experiences using these languages in a professional setting.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about us and what we do!
How to prepare for a job interview at ProPharma Group
✨Know Your Protocols
Make sure you’re well-versed in the study protocols and Good Clinical Practices (GCP). Brush up on the specific regulations that apply to the role, as this will show your potential employer that you’re serious about compliance and quality in clinical research.
✨Showcase Your Communication Skills
Since excellent verbal and written communication skills are a must, prepare to demonstrate these during the interview. Think of examples where you effectively communicated complex information to site personnel or stakeholders, and be ready to discuss how you handle training and presentations.
✨Highlight Your Technical Proficiency
Familiarise yourself with the tools mentioned in the job description, like EDC, CTMS, and eTMF systems. Be prepared to discuss your experience with Microsoft Office applications, especially how you've used them to create reports and presentations in past roles.
✨Demonstrate Organisational Skills
Prepare to talk about how you prioritise tasks and manage your workload. Share specific examples of how you’ve successfully planned and executed monitoring visits or managed multiple sites, showcasing your attention to detail and organisational prowess.