Principal Clinical Data Manager

Nacuity Pharmaceuticals, Inc. is a clinical-stage leader dedicated to developing innovative treatments that address oxidative stress, a key factor in severe chronic conditions and blinding eye diseases. Our cutting-edge therapies aim to halt oxidative tissue damage, with clinical programs focused on retinitis pigmentosa, cataract, and cystinosis. Our mission is to expand the science and clinical potential of treatments that tackle diseases involving oxidative stress, a largely unaddressed mechanism contributing to various ailments, both rare and common. Based in Fort Worth, TX, Nacuity is founded by experienced professionals from Alcon Laboratories and backed by esteemed organizations like the Foundation Fighting Blindness and RD Fund. The Principal Clinical Data Manager provides strategic leadership and oversight of clinical data management activities across multiple programs. This role manages a team of data managers, ensuring high-quality data collection, transformation, and submission in compliance with regulatory standards. The Principal Clinical Data Manager serves as the lead contact for data management, collaborating cross-functionally with key stakeholders to drive efficient processes, maintain data integrity, and uphold industry best practices. Additionally, they act as the data steward, ensuring proper governance, documentation, and inspection readiness for all clinical data.

Responsibilities

• Lead data management activities, ensuring accuracy, consistency, and compliance with regulatory standards.
• Oversee database build activities, data collection, coding, cleaning, and database lock.
• Develop and execute data management plans, including risk management strategies.
• Work closely with internal and external stakeholders, including Biostatistics, Clinical Development, Quality Assurance, and Regulatory Affairs, to facilitate seamless data flow and compliance.
• Serve as the primary data management contact for assigned therapeutic areas, ensuring proper planning and issue resolution.
• Ensure timely and quality deliverables within project timelines and budget constraints.
• Develop and implement validation checks, conduct data reviews, and resolve data discrepancies to maintain high data standards.
• Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, FDA regulations, and CDISC standards.
• Supervise database development, validation, and transfer processes in accordance with SOPs and regulatory requirements.
• Provide subject matter expertise in clinical data management systems, electronic data capture (EDC) platforms, and data standards such as CDISC.
• Develop and manage electronic Case Report Forms (eCRFs), data transfer specifications, and validation reports.
• Establish and refine data management standard operating procedures (SOPs) and best practices.
• Mentor and train junior data managers, fostering a collaborative environment and continuous learning culture.
• Ensure direct reports have adequate training and skills to meet regulatory and company standards.
• Guide teams on clinical data management best practices and evolving industry requirements.
• Maintain GCP inspection readiness by ensuring proper documentation and compliance with regulatory requirements.

• Bachelor’s degree in clinical, biological, or mathematical sciences, nursing, or a related field.
• Minimum of 6+ years of clinical data management experience in pharmaceutical development or CRO environment.
• Extensive experience with clinical trials, EDC databases, IRT systems, and diary applications for data collection.
• Strong knowledge of GCP, ICH, FDA, and CDISC regulatory requirements governing clinical studies.
• Proven ability to develop SOPs, risk management strategies, and data management plans.
• Demonstrated leadership, problem-solving, and project management skills.
• Excellent organizational, communication, and collaboration skills with a team-oriented approach.
• Self-motivated with a commitment to high-quality, on-time deliverables.

• Health Care Plan (Medical, Dental & Vision)
• Retirement Plan (401k, IRA)
• Life Insurance (Basic, Voluntary & AD&D)
• Paid Time Off (Vacation, Sick & Public Holidays)
• Family Leave (Maternity, Paternity)
• Training & Development
• Work From Home