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- Tasks: Lead early-phase oncology clinical trials and collaborate with cross-functional teams.
- Company: Myricx is a pioneering biotech firm focused on innovative cancer therapies.
- Benefits: Enjoy remote work options, a dynamic team environment, and the chance to make a real impact.
- Why this job: Join a rapidly growing company and shape the future of cancer treatment from day one.
- Qualifications: BSc or MSc in Life Sciences with experience in early-phase oncology clinical trials required.
- Other info: Myricx values diversity and fosters an inclusive workplace culture.
The predicted salary is between 60000 - 84000 £ per year.
Myricx is a pioneering global biotech company advancing innovative antibody-drug conjugates (ADCs) that deliver inhibitors of N-myristoyltransferase (NMT). We are a small but rapidly growing team, with a vision to advance a pipeline of ADCs based on our novel NMTi payload chemistry platform. This novel mechanism-of-action holds significant promise for treating cancer and other diseases. As leaders in NMT biology and pharmacology, Myricx successfully raised £90 million ($114 million) in Series A financing in 2024 to advance our pipeline of ADC therapeutics.
We are recruiting for a Senior Clinical Development Scientist who will be responsible for the scientific oversight and execution of early-phase oncology clinical trial(s).
Role Overview: The Clinical Development Scientist will collaborate closely with cross-functional teams to drive the development of novel oncology therapies. The successful candidate will have strong experience in clinical trial design, protocol development, scientific data interpretation, and CRO management, and will also be responsible for medical monitoring duties. This role requires a highly motivated, detail-oriented professional with a strong scientific background.
Key Responsibilities:
- Clinical Trial Support: Support the clinical development plan, including the planning and execution of clinical trials. Collaborate with clinical teams, CROs, and investigators to ensure scientific rigour and effective trial conduct. Author and revise essential clinical trial documents, including protocols, informed consent forms (ICFs), patient information sheets (PIS), trial-specific guidelines, and clinical study reports. Ensure that all documents are compliant with regulatory requirements, ethical standards, and company SOPs.
- CRO Management: Serve as the point of contact for CROs, ensuring high-quality execution of clinical trials. Participate in CRO selection and provide input during the vendor evaluation process. Participate in the management of scientific aspects of the CRO relationship including ensuring appropriate personnel and training.
- Data Analysis and Interpretation: Analyse/Visualise emerging clinical trial data using current software tools. Interpret/present scientific data from ongoing clinical trials to inform decision-making and identify potential issues. Summarise data and present to internal and external stakeholders, including data safety monitoring boards (DSMBs). Identify trends and address any data issues in emerging clinical trial databases.
- Medical Monitoring and Safety Oversight: Contribute to the medical monitoring of clinical trials, including review of safety data. Collaborate with the project medical monitor and safety teams to identify and evaluate any potential safety signals. Participate in safety data reviews and contribute to the management of serious adverse events (SAEs).
- Scientific Expertise: Maintain knowledge of the current literature in relevant therapeutic areas.
Requirements:
- BSc or MSc in Life Sciences (e.g. biology, pharmacology, or related studies).
- Demonstrated considerable experience in early-phase development, including executing Phase 1/2 oncology clinical trials.
- Experience with regulatory submissions (e.g. IND, BLA, MAA).
- Excellent scientific writing and proven ability to lead the development of clinical documents including trial protocols, ICFs, PIS, and others.
- Strong experience working with CROs.
- Experience managing or overseeing clinical trials in international regions.
- Knowledge of GCP, ICH guidelines.
- Experience with EDC systems, eCRFs and other clinical trial technologies.
- Experience with multiple cancer indications, and knowledge of cancer biology.
What’s in it for you? Why work at Myricx: We are a small but rapidly growing team, with a vision to advance a pipeline of ADCs based on our novel NMT inhibitor (NMTi) payload chemistry platform to address serious unmet needs in oncology. As an early joiner, you will have a unique opportunity to help shape our trajectory and make real impact from day one. Myricx Bio is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Seniority level: Not Applicable
Employment type: Full-time
Job function: Science
Senior Clinical Development Scientist employer: Myricx Bio
Contact Detail:
Myricx Bio Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Development Scientist
✨Tip Number 1
Network with professionals in the biotech and oncology fields. Attend industry conferences, webinars, or local meetups to connect with individuals who may have insights into Myricx or similar companies. Building relationships can often lead to referrals or insider information about job openings.
✨Tip Number 2
Stay updated on the latest advancements in antibody-drug conjugates and oncology therapies. Follow relevant journals, blogs, and news outlets to demonstrate your knowledge during interviews. This will show your genuine interest in the field and the company’s mission.
✨Tip Number 3
Prepare to discuss your experience with clinical trial design and CRO management in detail. Be ready to provide specific examples of how you've successfully collaborated with cross-functional teams and managed trials, as this is a key aspect of the role.
✨Tip Number 4
Familiarise yourself with the regulatory landscape, especially regarding IND, BLA, and MAA submissions. Understanding these processes will not only help you in the role but also impress the hiring team at Myricx, showing that you are well-prepared for the challenges ahead.
We think you need these skills to ace Senior Clinical Development Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trial design and execution, particularly in oncology. Emphasise your scientific writing skills and any previous work with CROs.
Craft a Compelling Cover Letter: In your cover letter, express your passion for advancing cancer therapies and detail how your background aligns with the responsibilities of the Senior Clinical Development Scientist role. Mention specific experiences that demonstrate your expertise in medical monitoring and data analysis.
Highlight Relevant Skills: Clearly outline your knowledge of GCP, ICH guidelines, and experience with EDC systems. This will show that you are well-versed in the regulatory landscape and clinical trial technologies.
Showcase Collaborative Experience: Since the role involves collaboration with cross-functional teams, provide examples of past teamwork in clinical settings. Highlight your ability to communicate effectively with various stakeholders, including CROs and investigators.
How to prepare for a job interview at Myricx Bio
✨Know Your Science
Brush up on the latest advancements in oncology and antibody-drug conjugates. Be prepared to discuss how your scientific expertise aligns with Myricx's focus on N-myristoyltransferase and its implications for cancer treatment.
✨Demonstrate CRO Management Skills
Highlight your experience working with Contract Research Organisations. Be ready to share specific examples of how you've successfully managed CRO relationships and ensured high-quality trial execution.
✨Showcase Your Clinical Trial Experience
Prepare to discuss your involvement in early-phase clinical trials, particularly Phase 1/2 studies. Be specific about your role in protocol development, data analysis, and any regulatory submissions you've handled.
✨Emphasise Team Collaboration
Since this role involves working closely with cross-functional teams, be ready to provide examples of how you've effectively collaborated with various stakeholders, including clinical teams and safety monitors, to drive successful outcomes.
