Principal Clinical Data Manager

Initial Therapeutics, Inc.; Malvern (Chester County); On-site; USD 80,000 - 130,000; Full time

Job summary

An established industry player is seeking a Principal Clinical Data Manager to lead and oversee clinical data management activities across multiple programs. This role requires strategic leadership to ensure high-quality data collection and compliance with regulatory standards. You will collaborate with cross-functional teams, drive efficient processes, and maintain data integrity. The ideal candidate will have extensive experience in clinical trials and a strong understanding of regulatory requirements. Join this dynamic team and make a significant impact in the field of clinical data management!

Qualifications

• 6+ years of clinical data management experience in pharmaceutical development.
• Strong knowledge of GCP, ICH, FDA, and CDISC regulatory requirements.
• Proven ability to develop SOPs and risk management strategies.

Responsibilities

• Lead data management activities ensuring accuracy and compliance.
• Oversee database build activities and data collection processes.
• Mentor junior data managers and maintain inspection readiness.

Skills

Clinical Data Management

Regulatory Compliance

Project Management

Data Quality Assurance

Team Leadership

Communication Skills

Education

Bachelor’s degree in clinical, biological, or mathematical sciences

Tools

EDC Platforms

IRT Systems

Data Management Systems

Job description

Job Purpose

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.
• Serve as the primary point of contact for data management activities during audits and inspections.
• Review and approve key project documents, including Data Management Manuals, CRF Completion Guidelines, and validation specifications.

Qualifications

• 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.

Ocugen is an equal opportunity employer. In order to provide equal employment and advancement opportunities to all individuals, we make all of our employment decisions based upon merit, qualifications, abilities, and an individual’s conduct and performance. We will not make any of our decisions, and will not discriminate against any employee or applicant, on the basis of race, color, religion, creed, national origin or ancestry, ethnicity, sex (including pregnancy), gender (including sexual orientation, gender identity and status as a transgender or transsexual individual), age, physical or mental disability, citizenship, past,
current or prospective service in the uniformed services, genetic information, or any other characteristic protected from discrimination under the law. Ocugen complies with applicable federal, state and local laws governing nondiscrimination in employment.