Sr. Data Manager

Sr. Data Manager - Temp to Hire

Note for Applicants: This position will begin as a full-time temporary assignment scheduled for 40 hours per week. The assignment is currently anticipated to continue through December 31, 2026, though timelines may change based on business needs and project demands. 
 
Depending on business needs, funding, and individual performance, there may be future consideration for extension or conversion to a regular full-time employee position. Conversion or extension is not guaranteed.  

Be Part of One Team, One Purpose.

At Emmes Group, we’re shaping the future of clinical research—where human intelligence meets cutting-edge technology to drive meaningful advancements in healthcare. With over 47 years of scientific excellence, we’ve led groundbreaking research in cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases, and neuroscience.

Through our two business units—Emmes, a full-service CRO, and Veridix AI, our technology, data, and analytical solutions —we are modernizing clinical trials and accelerating the development of life-changing therapies.

We believe that every clinical breakthrough starts with people—people who are passionate, purpose-driven, and ready to make an impact. At Emmes Group, we bring People, Science, and Technology together to collaborate with our customers and deliver global health impact. Our culture is built on integrity, collaboration, and innovation, ensuring that every challenge is met with perseverance and accountability.

The Senior Clinical Data Manager to oversee the collection, validation, and management of clinical trial data to ensure accuracy, integrity, and compliance with regulatory standards. The role involves leading data management activities, collaborating with cross functional teams, and ensuring the delivery of high quality data to support clinical study objectives.

• Lead the design, development, and implementation of clinical data management plans (CDMPs) and data handling procedures.
• Manage and monitor the collection, cleaning, and validation of clinical trial data to ensure accuracy and completeness.
• Oversee the setup and maintenance of electronic data capture (EDC) systems and data standards compliance (e.g., CDISC).
• Collaborate closely with clinical operations, biostatistics, medical writing, and regulatory affairs teams to support study timelines and deliverables.
• Serve as the primary data management liaison for clinical trials, providing guidance and support to study teams and external vendors.
• Participate in study start up meetings, data review meetings, and audit preparation.
• Ensure clinical data management activities comply with GCP, FDA, EMA, and other applicable regulations.
• Develop and implement data quality control procedures, discrepancy management, and data reconciliation.
• Support internal and external audits and inspections related to clinical data.
• Mentor and train junior data management staff.
• Manage relationships with external data vendors, CROs, and technology providers.
• Track project progress, resource allocation, and timelines.
• Performs other duties as assigned
• Complies with all policies and standards

• Bachelor's Degree Life Sciences, Nursing, Pharmacy, or related field; advanced degree. Required
• 4-6 years in clinical data management, preferably in pharmaceutical or CRO settings. Required
• 1-3 years Experience with global clinical trials and cross-functional team environments. Required
• Proficient with EDC systems as Medidata Rave, Oracle Clinical, REDCap. High
• Knowledge of clinical data standards such as CDISC SDTM, ADaM, and WHO Drug Dictionary. High
• Familiarity with clinical trial management systems, CTMS, and data visualization tools. High
• Strong understanding of regulatory guidelines as ICH GCP, FDA, EMA. High
• Excellent organizational and project management skills. High
• Strong attention to detail and problem solving ability. High
• Effective communication skills for interacting with multidisciplinary teams. High
• Ability to work independently and lead initiatives. High

If you’re looking for a career where your work advances global health and where scientific excellence meets real-world impact, join us and be part of something bigger. One Team, One Purpose.

CONNECT WITH US!
Find us on LinkedIn:/the-emmes-group/
Visit our website:https://www.theemmesgroup.com/