At a Glance
- Tasks: Conduct site monitoring and ensure data accuracy for innovative cancer treatments.
- Company: Join a leading biopharmaceutical company dedicated to transforming patient care.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic work environment with global impact and career advancement opportunities.
- Why this job: Make a real difference in patients' lives by working on groundbreaking drug development.
- Qualifications: Bachelor's degree in Life Sciences and oncology trial monitoring experience required.
The predicted salary is between 50000 - 70000 £ per year.
Inno Care (HKEX: 09969; SSE: 688428) is a commercial stage biopharmaceutical company committed to discovering, developing, and commercializing innovative drugs for the treatment of cancers and autoimmune disease, with unmet medical needs worldwide.
Inno Care has built up a fully integrated platform in terms of research and development, clinical development, manufacturing and commercialization.
To date, the Company has developed a robust product pipeline comprising three approved drugs (orelabrutinib, tafasitamab and zurletrectinib), and more than ten innovative drug candidates in clinical development, and multiple programs in preclinical stages.
Inno Care has successfully got listed on both Hong Kong Stock Exchange and the STAR Board of Shanghai Stoch Exchange.
Our world-class team exhibits remarkable synergy and efficient execution, with entrepreneurial spirit, which has made outstanding achievements in innovation, commercialization and globalization.
If you would like to join us, we will develop innovative drugs for the benefit of patients worldwide. Website link: https://www. innocarepharma. com/en. Linked
In: Inno Care Pharma.
- Key Responsibilties
- Conduct site selection, initiation, routine monitoring, and close-out visits per ICH-GCP and study-specific monitoring plans.
- Perform source data review (SDR), source data verification (SDV), and CRF review to ensure data accuracy and completeness.
- Manage site performance, including patient recruitment, retention, and issue resolution.
- Oversee investigational product (IP) accountability, storage, and handling at sites.
- Ensure timely collection and filing of essential documents in e TMF, maintaining audit readiness.
- Apply oncology-specific knowledge including RECIST 1.1 and CTCAE grading for adverse event and tumor response monitoring.
- Track and report SAEs, protocol deviations, and escalate compliance issues as needed.
- Prepare and finalize monitoring visit reports within required timelines using CTMS.
- Serve as primary site contact, building strong site partnerships.
- Collaborate with Data Management, Drug Safety, and cross-functional study teams.
Requirements
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
- Minimum 2–3 years of on-site CRA monitoring experience in a CRO, pharma, or biotech.
- Minimum 2 years of direct oncology trial monitoring experience (Phase I–III/IV) – non-negotiable.
- Solid knowledge of ICH-GCP, FDA regulations, and US clinical research requirements.
- Familiarity with RECIST criteria and CTCAE grading system.
- Proficiency with CTMS, e TMF, EDC, and IWRS/IVRS.
- Strong written/verbal communication skills in English. Mandarin (spoken) – a plus
- This job is locate in China or USA
Clinical Research Associate in Worcester employer: InnoCare Pharma
InnoCare is an exceptional employer that fosters a dynamic and innovative work culture, dedicated to advancing healthcare through cutting-edge biopharmaceutical research. Employees benefit from a collaborative environment that encourages professional growth and development, with opportunities to contribute to groundbreaking projects in oncology and autoimmune disease treatment. Located in China or the USA, InnoCare offers a unique chance to be part of a world-class team making a significant impact on patient lives globally.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate in Worcester
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like InnoCare Pharma.
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We think you need these skills to ace Clinical Research Associate in Worcester
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at InnoCare Pharma!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show InnoCare Pharma that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at InnoCare Pharma!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At InnoCare Pharma, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at InnoCare Pharma
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at InnoCare Pharma that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with InnoCare Pharma’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
