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Director of Clinical Research, Clinical Development

SAGA is seeking a talented and highly motivated Director of Clinical Research with a strong interest in advancing our mission to revolutionize cancer diagnostics through the use of liquid biopsies.

 You will be a key member of the SAGA clinical development team, an international multi-disciplinary team, where you will be responsible for providing technical and genomic expertise to key clinical studies and biopharma projects.  The trials and clinical studies may be either sponsored by SAGA or conducted in collaboration with academic, or commercial partners.  We are growing our clinical development team and engaging with world leading KOLs and so this a unique opportunity to build the clinical research, reporting to the VP of Clinical Development.

 This is an exciting opportunity to join a rapidly scaling cancer genomics startup with excellent momentum, international attention, and strong customer traction – where every role is critical. Through cooperation and teamwork, you will have the opportunity to help grow the company and make a real difference for people with cancer worldwide.

Key responsibilities:

  • Work with external research collaborators from leading academic centers globally to manage relationships, project timelines, sample forecasting and tracking, and data management and analysis for clinical studies.
  • Manage proposals from external collaborators through to successful contract execution.
  • Act as a point person for an internal clinical team and site staff. Communicate with the larger research and development team regarding research/analysis to ensure understanding of design and results. Provide laboratory expertise to clinical development projects as required.
  • Develop clear and measurable analytical plans.
  • Interpret individual testing results and provide compilation of all analytical data for finalization and approval prior to clinical study analysis.  Utilize primary statistical analysis methods.
  • Keep up to date with scientific and academic research data and provide summaries and reviews.
  • Provide expertise in cancer genomics for the development of new products.
  • Prepare data presentations and publications as required to promote SAGA clinical studies and products. Attend scientific meetings to represent SAGA and support opportunities for abstracts, posters and podium presentation.
  • Provide scientific support for biopharma & other business development activity as required.
  • Maintain study budget for individual collaborations.  Understand, implement and verify complex and tailored study budgets or invoicing for projects.
  • Some travel will be required for this position (approximately 10%)

 

Technical Requirements:

  • PhD or equivalent in Cancer Genomics or similar field. 
  • 5+ years experience working in a molecular biology environment.   .
  • Experience of research/clinical trials in the oncology field, would be an advantage.
  • Computer literacy (including relevant software, such as Excel, Word, PowerPoint, Adobe plus specific regulatory packages)
  • Experience in conducting statistical analysis of genomic datasets is desirable.
  • Experience in a Biotech/start-up environment would be advantageous.

Skill Requirements:

  • Extensive Molecular biology skills.
  • Detailed knowledge of Cancer Genomics.
  • Excellent English oral and written communication skills, including experience in giving presentations.
  • Knowledge of Product Development would be an advantage.
  • Strong troubleshooting and data interpretation skills.  Application of statistical principles and analysis skills.
  • Experienced in clinical research.
  • Strong team working skills with a proven track record of working collaboratively to ensure delivery of projects to meet challenging timelines.
  • Flexibility towards work assignments, new learning and travel.

What we offer:

  • The opportunity to build a critical clinical research portfolio from concept and develop exceptional data packages.
  • As an early employee of the clinical research team, you will be involved in many aspects of the business and help set the direction/culture as we grow.
  • You will be given the autonomy and resources to deliver to the highest level.
  • All the perks of a start-up – highly competitive salaries, flexible working, flat structure, and a dynamic work environment.

Benefits

  • Generous benefits package including medical, dental, vision, FSA, HRA, and paid parental leave.
  • Membership to SAGA’s Equity scheme.   

 

Primary location: Remote with regular visits to Morrisville NC office as needed

SAGA Diagnostics is an equal opportunity employer, fully committed to achieving a diverse and inclusive workplace that embraces and encourages applicants of every background.  The company’s policy regarding equal employment opportunity means that all decisions regarding recruitment, hiring, benefits, wage and salary administration, scheduling, disciplinary action and termination will be made without unlawful discrimination on the basis of sex, gender, race, color, age, national origin, religion, disability, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, citizenship status, pregnancy or maternity, veteran status, or any other status protected by applicable federal, state or local law.

Average salary estimate

$135000 / YEARLY (est.)
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$150000K

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What You Should Know About Director of Clinical Research, Clinical Development, SAGA Diagnostics

SAGA is on the hunt for a passionate and highly skilled Director of Clinical Research to join our Clinical Development team. If you're keen on making a tangible impact in the realm of cancer diagnostics using innovative liquid biopsies, this role is for you! As a pivotal member of our interdisciplinary team, you will leverage your technical and genomic expertise to drive essential clinical studies and biopharma projects, either led by SAGA or in partnership with academic and commercial collaborators. With the opportunity to work alongside prominent key opinion leaders in the field, you'll play a vital role in shaping our clinical research landscape. Your responsibilities will span managing relationships with research partners globally, overseeing project timelines, and ensuring comprehensive data management and analysis. You’ll also interpret testing results and support the development of groundbreaking products in cancer genomics. Plus, this is your chance to represent SAGA at scientific meetings, showcasing our research to the wider community! We’re excited to offer a dynamic and flexible work environment as well as a chance to help steer the direction of our growing clinical research team. If you have a PhD in Cancer Genomics or a related field, extensive molecular biology skills, and a strong collaborative spirit, we want to hear from you. Join us, and let's make a difference in the fight against cancer together!

Frequently Asked Questions (FAQs) for Director of Clinical Research, Clinical Development Role at SAGA Diagnostics
What are the primary responsibilities of the Director of Clinical Research at SAGA?

As the Director of Clinical Research at SAGA, your key responsibilities will involve managing clinical studies and biopharma projects, developing relationships with external research collaborators, and ensuring successful execution of research proposals. You'll be tasked with providing laboratory expertise, interpreting testing results, and developing analytical plans. Additionally, you'll represent SAGA at scientific meetings and support biopharma activities, making your role both impactful and dynamic!

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What qualifications are required for the Director of Clinical Research position at SAGA?

To qualify as the Director of Clinical Research at SAGA, candidates must possess a PhD or equivalent in Cancer Genomics or a similar field, along with 5+ years of experience in a molecular biology environment. Experience in clinical trials within the oncology field is advantageous, as are strong data interpretation skills and proficiency in statistical analysis of genomic datasets. Strong communication skills and a collaborative mindset are also essential for success in this role.

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What is the work environment like for a Director of Clinical Research at SAGA?

At SAGA, the work environment for the Director of Clinical Research is energetic and fast-paced, characteristic of a thriving startup. This position allows for remote work along with regular visits to our Morrisville NC office, fostering flexibility and autonomy. As part of an international team, you'll be deeply involved in diverse projects that directly contribute to our mission of revolutionizing cancer diagnostics through advanced technology.

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How does SAGA support the professional growth of its Director of Clinical Research?

SAGA is committed to supporting the professional development of its Director of Clinical Research by providing autonomy, resources, and the ability to shape project direction. As an early member of the clinical research team, you will have platforms to enhance your skills and expertise, lead key projects from concept to execution, and build a critical clinical research portfolio—all while making significant contributions towards cancer treatment advancements.

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What benefits does SAGA offer to its Director of Clinical Research?

SAGA offers a generous benefits package for the Director of Clinical Research, including medical, dental, and vision coverage, as well as flexible spending accounts and paid parental leave. Additionally, employees can gain membership to SAGA's Equity scheme, ensuring you're recognized as part of our collective success. The startup culture here emphasizes competitive salaries, a flat structure, and a dynamic work environment that promotes work-life balance.

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Common Interview Questions for Director of Clinical Research, Clinical Development
Can you explain your experience with clinical trials in oncology?

When answering this question, focus on the specific roles you've played in clinical trials. Discuss your involvement in study design, data collection, analysis, or project management. Share examples of successful trials you’ve worked on, highlighting your ability to collaborate and deliver results while emphasizing any statistical methods or genomic studies you've utilized.

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How do you prioritize tasks in a fast-paced research environment?

Highlight your organizational skills and methodologies for prioritization, such as creating logical timelines, setting clear goals, and utilizing project management tools. Share specific examples where you handled multiple projects simultaneously, focusing on how you ensured timely delivery while maintaining quality standards.

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Describe a situation where you successfully collaborated with external research collaborators.

Discuss a specific collaboration that showcases your ability to build relationships with external partners. Detail how you managed communication, tracked progress, and resolved any conflicts or challenges that arose during the project, emphasizing the positive outcomes that resulted from effective collaboration.

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What strategies do you use for statistical analysis of genomic datasets?

Talk about specific software tools you are familiar with and your approach to statistical analysis, including any methodologies you prefer. Mention how you ensure the accuracy and reliability of your results, and if applicable, include outcomes that arose from your analysis.

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How do you keep up with the latest research in cancer genomics?

Emphasize your commitment to continuous learning through attending scientific meetings, subscribing to relevant journals, and engaging with professional networks. Provide examples of how you’ve implemented new findings into your work, demonstrating your proactive approach to integrating contemporary research into practical applications.

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Can you give an example of a successful analytical plan you've developed?

Describe a specific analytical plan that you crafted, detailing the objectives, the methodologies employed, and the outcomes achieved. Highlight the importance of measurable goals and how your analytical approach contributed to the overall success of the clinical study.

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What role do you believe communication plays in clinical research?

Articulate the importance of clear and effective communication within multidisciplinary teams and between collaborators. Discuss how fostering open communication can enhance teamwork, facilitate problem-solving, and ultimately contribute to the success of clinical research projects.

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How do you approach problem-solving in research settings?

Share your problem-solving process, which may include analyzing the situation, identifying possible solutions, and selecting an appropriate course of action. Provide examples of challenges you've faced and the steps you took to overcome them, focusing on the skills that led to successful resolution.

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Discuss how you manage project budgets while maintaining research quality.

Elaborate on your experience with budgeting, emphasizing your ability to plan, track expenses, and adjust as necessary without compromising the integrity of the research. Mention any software or tools you're proficient in for managing budgets and how you ensure projects stay within financial constraints.

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What motivates you to work in cancer research?

Convey your passion for making a meaningful impact in the field of cancer research. Discuss any personal or professional experiences that drive your commitment to advancing cancer diagnostics and how these motivations align with SAGA's mission to improve patient outcomes through innovative approaches.

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SAGA Diagnostics AB is a personalized cancer diagnostics and disease monitoring company that offers molecular genetic testing of tissue biopsies and non-invasive "liquid biopsies" such as blood samples.

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DATE POSTED
December 24, 2024

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