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Title
Text copied to clipboard!Clinical Research Scientist
Description
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We are looking for a Clinical Research Scientist to join our dynamic team and contribute to the advancement of medical science through the design, execution, and analysis of clinical trials. The ideal candidate will have a strong background in clinical research methodologies, regulatory compliance, and data interpretation. This role involves close collaboration with cross-functional teams including medical affairs, regulatory affairs, biostatistics, and clinical operations to ensure the successful development and implementation of clinical studies.
As a Clinical Research Scientist, you will be responsible for developing clinical study protocols, overseeing trial execution, and ensuring data integrity and compliance with Good Clinical Practice (GCP) guidelines. You will also play a key role in interpreting clinical data, preparing study reports, and contributing to scientific publications and regulatory submissions.
This position requires excellent analytical skills, attention to detail, and the ability to manage multiple projects simultaneously. Strong communication skills are essential, as you will be expected to present findings to internal stakeholders and external partners, including regulatory agencies and scientific communities.
The successful candidate will be passionate about improving patient outcomes and advancing healthcare through evidence-based research. You should be comfortable working in a fast-paced environment and be committed to maintaining the highest standards of scientific integrity and ethical conduct.
If you are a motivated and detail-oriented professional with a passion for clinical research, we encourage you to apply and become a part of our mission to bring innovative therapies to patients worldwide.
Responsibilities
Text copied to clipboard!- Design and develop clinical study protocols and case report forms
- Coordinate and oversee clinical trial execution
- Ensure compliance with regulatory requirements and GCP guidelines
- Analyze and interpret clinical trial data
- Prepare clinical study reports and scientific publications
- Collaborate with cross-functional teams including medical, regulatory, and biostatistics
- Support regulatory submissions and responses
- Monitor trial progress and address issues proactively
- Maintain accurate and complete study documentation
- Present research findings to internal and external stakeholders
Requirements
Text copied to clipboard!- Master’s or PhD in life sciences, pharmacy, or related field
- Minimum 3 years of experience in clinical research
- Strong knowledge of clinical trial design and methodology
- Familiarity with regulatory guidelines (FDA, EMA, ICH-GCP)
- Excellent analytical and problem-solving skills
- Proficient in data analysis software and clinical databases
- Strong written and verbal communication skills
- Ability to manage multiple projects and meet deadlines
- Attention to detail and high level of accuracy
- Team player with strong interpersonal skills
Potential interview questions
Text copied to clipboard!- What experience do you have in designing clinical trials?
- How do you ensure compliance with GCP and regulatory guidelines?
- Describe a challenging clinical study you worked on and how you overcame obstacles.
- What data analysis tools are you proficient in?
- How do you handle tight deadlines and multiple projects?
- Have you contributed to any regulatory submissions or scientific publications?
- What therapeutic areas have you worked in?
- How do you ensure data integrity in clinical trials?
- Describe your experience working with cross-functional teams.
- What motivates you to work in clinical research?
