Senior Clinical Data Manager

BioSpace; Malvern (Chester County); On-site; USD 120,000 - 160,000; Full time

Job summary

Ocugen is seeking a Senior Clinical Data Manager to lead data management efforts, oversee quality data collection, and drive critical data handling activities for clinical development programs and marketed products.

The candidate will provide leadership to junior staff, work with cross-functional teams, and ensure high-quality, timely deliverables while maintaining regulatory compliance and data standards.

Qualifications

• BS degree in clinical/biological/mathematical sciences, or nursing or equivalent.
• 5–7 years of clinical data management experience in biopharma or CRO.
• Experience with CRFs and development of EDC databases, IRT systems and diary apps.
• Veeva experience is preferred.
• Strong knowledge of GCP, ICH, FDA and CDISC regulatory requirements.
• Excellent attention to detail and timely deliverables.

Responsibilities

• Oversee studies or a program, mentor team members, and manage vendors.
• Make high-level decisions on data standards and risk-based management strategies.
• Lead inspection readiness and ensure document completeness across studies.
• Serve as SME during audits and guide SOP alignment with compliance expectations.
• Provide strategic input to Clinical Operations, Biostatistics, Programming and Quality on data flow and improvements.
• Lead the development and execution of data management plans (DMPs) and eCRF design.
• Collaborate with Biometrics, Clinical and Regulatory to implement protocols and data outputs.
• Develop and validate edit checks and validation reports to ensure data quality.
• Prepare for audits and ensure data management processes meet standards.

Skills

Clinical data management experience

CRFs and EDC development

GCP/ICH/FDA/CDISC knowledge

Attention to detail

Communication and collaboration

Veeva experience

Education

BS degree in clinical/biological/mathematical sciences or nursing

Job description

Position Summary

The Senior Clinical Data Manager plays a pivotal role within Ocugen’s clinical data management team. This individual will lead data management efforts, oversee quality data collection and management processes, and contribute to critical aspects of clinical trial data handling, including database design, CRF development, data monitoring, and validation for clinical development programs and marketed products. In addition to technical responsibilities, the Senior Clinical Data Manager will provide leadership to junior data management staff and work collaboratively across functional teams, ensuring high-quality and timely deliverables.

Description

The Senior Clinical Data Manager plays a pivotal role within Ocugen’s clinical data management team. This individual will lead data management efforts, oversee quality data collection and management processes, and contribute to critical aspects of clinical trial data handling, including database design, CRF development, data monitoring, and validation for clinical development programs and marketed products. In addition to technical responsibilities, the Senior Clinical Data Manager will provide leadership to junior data management staff and work collaboratively across functional teams, ensuring high-quality and timely deliverables.

Responsibilities

• Oversee studies or a program, ensures cross study consistency, mentors team members, and manage vendors as needed.


• Makes higher level decisions on data standards, risk based data management strategies, and protocol driven design choices.


• Leads inspection readiness, ensures documentation completeness across studies,


• Serves as a subject matter expert during audits, helps standardize SOP alignment, guides the team in applying GCP, ICH, CDISC, and internal compliance expectations.


• Provides strategic input to Clinical Operations, Biostatistics, Programming, and Quality on data flow, database design improvements, standards adoption, and process optimizations.


• Represents DM in program level meetings and drives improvements across studies (aligned with broader responsibilities seen in senior and principal level descriptions).


• Provide mentorship and technical guidance to junior data management staff.


• Ensure accurate and efficient collection of electronic clinical trial data.


• Develop and validate edit checks and validation reports to maintain the highest quality data.


• Ensure all required documentation is completed accurately and promptly across studies.


• Develop and implement innovative data strategies to streamline data management workflows.


• Identify and mitigate risks in data management processes proactively.


• Take the lead on special projects and additional tasks as required by management.


• Lead the development and execution of data management plans (DMPs), ensuring seamless data flow from collection to final analysis.


• Design and oversee program standards and study-specific electronic Case Report Forms (eCRFs).


• Partner with Biometrics, Clinical, and Regulatory teams to implement research protocols and ensure proper clinical data outputs for deliverables.


• Develop and manage data transfer specifications, data review plans, and risk management strategies.


• Collaborate on cross-functional project timelines and ensure database deliverables are achieved within schedule and quality standards.


• Author and revise standard operating procedures (SOPs) and study-specific DMPs.


• Prepare for and participate in audits, ensuring data management processes meet compliance standards.

Qualifications

• BS degree in clinical, biological or mathematical sciences, or related field, or nursing qualification, or work- related equivalent.


• 5-7 years of clinical data management experience in biopharma or CRO environment.


• Strong attention to detail and motivation to provide quality deliverables.


• Able to work in a fast-paced environment.


• Experience with clinical trials.


• Experience with CRFs, and in the development process of EDC databases, IRT systems and diary applications for data collection. Veeva experience is preferred.


• Strong knowledge of GCPs, ICH, FDA, and CDISC regulatory requirements governing clinical studies.


• Demonstrated attention to detail and outstanding organization skills.


• Self-motivated with a commitment to high quality, on-time deliverables.


• Excellent communication and collaboration skills with a team-oriented approach.


• Demonstrated ability to identify and resolve issues and effectively manage timelines.

Working Conditions

This position operates in an office setting, in person. Remote work will be limited. Job may additionally require incumbent to be available outside of these hours to handle priority business needs.