Clinical Scientist Immunology
WFA Digital Insight
The demand for skilled clinical scientists in immunology has seen significant growth, with a focus on innovative treatments and collaborative research environments. Excelya, with its audacious approach to healthcare, stands out by combining passion for science with teamwork, making it an attractive opportunity for those seeking a challenging role in a forward-thinking company. As the industry continues to evolve, candidates with strong experience in clinical studies, particularly in immunology and inflammation, are in high demand. With the remote job market expanding, this role offers the chance to be part of a dynamic team without geographical constraints, contributing to the development of new treatments and improving patient outcomes.
Job Description
About the Role
As a Clinical Scientist Immunology at Excelya, you will be at the forefront of clinical study planning, execution, analysis, and reporting. This role is pivotal in supporting the Study Medical Manager throughout the clinical study lifecycle, ensuring high-quality clinical trial delivery in compliance with regulatory requirements. Your expertise will contribute to the development and review of key clinical documents and the performance of medical reviews of patient data.The immunology field is rapidly advancing, with groundbreaking treatments emerging regularly. Your involvement in this area will not only contribute to the advancement of medical science but also improve the lives of patients worldwide. Excelya's commitment to innovation, care, and energy creates a dynamic environment where your skills and experience will be valued and utilized to their fullest potential.
Working as part of a cross-functional team, you will collaborate closely with various departments, including Clinical Operations, Pharmacovigilance, Biostatistics, and Data Management. Your strong understanding of clinical development, study design, and clinical trial conduct will be essential in driving the success of clinical studies. The role requires a high level of fluency in English, both written and spoken, as well as excellent cross-functional collaboration and communication skills.
What You Will Do
- Support and represent the Study Medical Manager throughout the clinical study lifecycle
- Contribute to the development and review of key clinical documents, including protocols, protocol amendments, informed consent forms (ICFs), CRFs, and medical data validation plans
- Perform medical review of patient data, listings, narratives, CIOMs, and clinical cases
- Collaborate closely with Clinical Operations, Pharmacovigilance, Biostatistics, and Data Management teams to support data review and consistency checks
- Review study-related documentation and contribute to interim analyses, Clinical Study Reports (CSRs), publications, and statistical outputs
- Support the preparation and management of study committees, investigator meetings, and study training activities
- Maintain medical and scientific documentation within the Trial Master File (TMF)
- Draft responses to medical questions from Health Authorities, Ethics Committees, investigators, and study teams
- Develop medical review guidelines and support outsourced medical review activities when applicable
- Contribute to audit and inspection readiness activities and support responses to findings
What We Are Looking For
- Advanced degree in Medicine (MD), Pharmacy (PharmD), Life Sciences, or related scientific discipline
- Strong experience as a Clinical Scientist, Medical Scientist, Clinical Research Physician, or similar role
- Experience supporting clinical studies in Immunology & Inflammation and/or Oncology
- Strong understanding of clinical development, study design, and clinical trial conduct
- Knowledge of ICH-GCP, regulatory requirements, and clinical research processes
- Experience reviewing clinical data, patient profiles, narratives, and safety information
- Familiarity with Clinical Study Reports (CSRs), protocols, and TMF documentation
- Strong cross-functional collaboration and communication skills
- Fluency in English, written and spoken
Nice to Have
- Experience with Excel and other data management tools
- Knowledge of statistical analysis and data interpretation
- Certification in clinical research or a related field
- Experience working in a remote or global team environment
Benefits and Perks
- Opportunity to work with a dynamic and ambitious healthcare company
- Collaborative and supportive work environment
- Professional development and growth opportunities
- Contribution to the development of innovative treatments and improvement of patient outcomes
- Competitive compensation package
- Flexible working hours and remote work options
- Access to leading-edge technology and tools
- Comprehensive health and wellness programs
- Recognition and reward for outstanding performance
How to Stand Out
- Ensure your CV and cover letter are tailored to highlight your experience in immunology and clinical studies, emphasizing your skills in data analysis and medical writing.
- Prepare to discuss your understanding of regulatory requirements and clinical research processes during the interview.
- Showcase your ability to work collaboratively in a cross-functional team environment and your fluency in English.
- Be ready to provide examples of your experience in developing and reviewing clinical documents and performing medical reviews of patient data.
- Consider creating a portfolio of your work, including any publications or presentations you have made in the field of immunology.
- During salary negotiation, highlight your unique skills and experience, and be prepared to discuss your expectations based on industry standards.
- Look for red flags such as lack of transparency about the company culture, unrealistic expectations about workload, or poor communication from the hiring team.
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