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Director, Clinical Data Management

More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks. With our purified, high-precision investigational cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives.


The Director of Clinical Data Management will lead Orca Bio's data management function, ensuring the highest standards of data integrity across all clinical programs. This role combines strategic leadership with operational expertise to deliver high-quality clinical data solutions that drive decision-making and regulatory submissions.


Responsibilities
  • Clinical Data Strategy & Operations:
  • Design and implement comprehensive clinical data strategies aligned with Orca Bio's development objectives
  • Lead data management team in all aspects of clinical data management from study startup through database lock for multiple concurrent studies
  • Establish robust data collection, cleaning, and validation processes that ensure data integrity
  • Direct database design, build, and maintenance activities with a focus on quality and efficiency
  • Oversee query management, data reconciliation, and database lock procedures
  • Develop and implement data quality management systems that ensure accuracy and reliability
  • Establish data standards and processes based on CDASH/SDTM and other industry standards
  • Ensure compliance with ICH guidelines, 21 CFR Part 11, and other relevant regulations
  • Author and maintain SOPs and work instructions for clinical data management
  • Implement risk-based quality management approaches to data oversight

  • Team Leadership & Development:
  • Mentor and develop a high-performing clinical data management team
  • Provide direction, guidance, and quality oversight to team members, including consultants and vendors to achieve corporate goals and milestones
  • Establish clear roles, responsibilities, and career development paths
  • Partner with Biostatistics, Clinical Operations, Regulatory Affairs, and Medical Affairs
  • Cultivate a culture of excellence, innovation, and continuous improvement
  • Represent data management in interactions with regulatory agencies and external partners
  • Manage relationships with data management vendors
  • Manage departmental resources, timelines, budget, and performance metrics
  • Provide leadership in recruiting, training, and retaining top talent


Qualifications & Experience
  • BSc or MSc in Life Sciences, Data/Computer Science, Bioinformatics or equivalent industry experience; advanced degree preferred
  • 10+ years of progressive experience in clinical data management, with at least 5 years in leadership
  • Comprehensive knowledge of clinical data management processes, systems, and regulatory requirements
  • Proven experience with EDC systems (Zelta EDC preferred) and medical coding dictionaries
  • Strong understanding of CDISC standards (CDASH, SDTM) and their implementation
  • Track record of successfully building and leading data management teams
  • Experience interacting with regulatory agencies regarding data management approaches
  • Background in programming or technical data systems preferred
  • Strategic thinker who can translate business objectives into actionable data strategies
  • Strong interpersonal skills, including verbal and written communication, are essential
  • Decisive problem-solver who can navigate complex challenges
  • Collaborative partner who builds effective relationships across functions
  • Entrepreneurial mindset; thrives in a fast-paced, evolving environment
  • Flexibility in responding to change or business needs; desire to improve upon established processes
  • Passionate about improving patient outcomes through rigorous clinical data practices


$200,000 - $225,000 a year

The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. You will also be eligible to receive pre-IPO equity, in addition to medical, dental, and vision benefits, flexible PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include free daily lunches and snacks at our on-site locations.


Who we are


We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them.


We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility.


We innovate on a path that hasn’t been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren’t afraid to ask “why not” and challenge the status quo.


We maintain a start-up culture of camaraderie and leadership by example, regardless of title.


We’re proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers.


Notice to staffing firms


Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment.

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Average salary estimate

$212500 / YEARLY (est.)
min
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$200000K
$225000K

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What You Should Know About Director, Clinical Data Management, Orca Bio

Are you ready to make a transformative impact in the field of biotechnology? At Orca Bio, we are on a mission to redefine the transplant process and improve the lives of blood cancer patients with our next-generation cell therapies. We’re seeking a Director, Clinical Data Management to join our team in Menlo Park, CA. In this pivotal role, you'll lead our data management function, ensuring the highest standards of data integrity across all clinical programs. You'll drive the design and implementation of comprehensive data strategies, oversee robust data collection and validation processes, and ensure compliance with industry regulations. Your leadership will guide a dynamic team through multiple concurrent studies, fostering a culture of excellence and innovation. We’re looking for someone with at least 10 years of progressive experience in clinical data management, including 5 years in a leadership role, along with strong interpersonal skills and a collaborative spirit. If you have a passion for improving patient outcomes and the skills to navigate complex challenges, we invite you to become part of our exciting journey. Join us at Orca Bio, where we innovate to unlock better quality of life for patients while maintaining a culture that values compassion, integrity, and entrepreneurial spirit. Together, we can make a real difference!

Frequently Asked Questions (FAQs) for Director, Clinical Data Management Role at Orca Bio
What are the primary responsibilities of the Director, Clinical Data Management at Orca Bio?

The Director, Clinical Data Management at Orca Bio is responsible for leading the data management team, ensuring data integrity across clinical programs, and implementing comprehensive data strategies aligned with the company’s objectives. This includes overseeing data collection processes, query management, and database lock procedures, as well as ensuring compliance with industry regulations like ICH guidelines and 21 CFR Part 11.

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What qualifications are required to apply for the Director, Clinical Data Management role at Orca Bio?

Candidates applying for the Director, Clinical Data Management position at Orca Bio should possess a BSc or MSc in Life Sciences, Data/Computer Science, or Bioinformatics, with an advanced degree preferred. Additionally, a strong background of at least 10 years in clinical data management, including 5 years in a leadership capacity, along with comprehensive knowledge of regulatory requirements and industry standards such as CDISC, is essential.

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How does the Director, Clinical Data Management contribute to patient outcomes at Orca Bio?

The Director, Clinical Data Management at Orca Bio plays a crucial role in enhancing patient outcomes by ensuring that clinical data management processes are rigorous and reliable. By leading the team to maintain high-quality and accurate clinical data, the Director helps support informed decision-making and regulatory submissions that ultimately positively impact patient care and treatment effectiveness.

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What type of experience is beneficial for the Director, Clinical Data Management role at Orca Bio?

Beneficial experience for the Director, Clinical Data Management position at Orca Bio includes a strong understanding of electronic data capture (EDC) systems, particularly Zelta EDC, as well as a background in programming or technical data systems. Candidates should also demonstrate a proven track record in building and leading effective teams and engaging with regulatory agencies regarding data management strategies.

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What is the work culture like at Orca Bio for the Director, Clinical Data Management?

The work culture at Orca Bio is dynamic and centered around the values of passion, courage, and integrity. As the Director, Clinical Data Management, you'll find an entrepreneurial spirit that encourages innovation and measured risk-taking. The environment promotes collaboration across various functions while fostering leadership and camaraderie among team members, regardless of their titles.

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Common Interview Questions for Director, Clinical Data Management
How do you ensure data integrity in clinical trials?

To ensure data integrity in clinical trials, I prioritize implementing robust data validation processes and establishing clear protocols for data collection and management. Regular audits and quality checks are integrated to catch any discrepancies early, while maintaining compliance with industry standards to safeguard data accuracy.

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Can you describe your experience with EDC systems?

I have extensive experience utilizing EDC systems, specifically Zelta EDC, to manage clinical data efficiently. My role involved configuring the system for specific studies, training team members on its features, and utilizing its reporting capabilities to track progress and identify potential data issues promptly.

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What strategies do you use to mentor your data management team?

I believe in a hands-on mentorship approach that includes regular one-on-one feedback sessions, fostering open communication, and encouraging professional development. I set clear expectations while also empowering team members to take ownership of projects, creating a culture of growth and accountability.

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How do you handle regulatory compliance in clinical data management?

Handling regulatory compliance involves staying informed on current guidelines such as ICH and 21 CFR Part 11, and ensuring our data management practices adhere to these standards. I emphasize training and continuous education for my team to promote a thorough understanding of compliance requirements in all phases of clinical data management.

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What is your approach to risk-based quality management?

My approach to risk-based quality management includes identifying areas of potential risk early in the project lifecycle and implementing proactive measures to mitigate them. This involves regular risk assessments and developing contingency plans, ensuring that our data management processes remain robust and compliant, even in the face of challenges.

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Can you explain your experience with CDISC standards?

I have a comprehensive understanding of CDISC standards such as CDASH and SDTM, which I have applied in previous clinical trials to standardize data collection and ensure regulatory compliance. Familiarity with these standards allows for efficient data sharing and submission processes.

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

In a fast-paced environment, I prioritize tasks by assessing their impact on project timelines and objectives. I utilize tools for task management and regularly communicate with my team to ensure that they have clarity on priorities, allowing flexibility when urgent issues arise.

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Describe a challenging project you led and how you overcame obstacles.

One challenging project involved a tight deadline for a complex data management task. I tackled this by reallocating resources, enhancing team collaboration, and proactively addressing potential bottlenecks. Through meticulous planning and open communication, we successfully delivered the project on time.

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What role does communication play in clinical data management?

Communication is vital in clinical data management as it ensures alignment among cross-functional teams. Regular updates, clear documentation, and open lines of communication help to address issues before they escalate and maintain data integrity throughout the study lifecycle.

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How do you stay current with industry trends in clinical data management?

I stay current with industry trends by attending conferences, participating in professional organizations, and networking with peers in the field. Remaining engaged with the latest research and technological advancements helps me adapt our data management practices effectively.

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Full-time, on-site
DATE POSTED
April 5, 2025

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