[Hiring] Associate Clinical Data Manager - Operations @Careers Signant Health

Role Description

The Associate Clinical Data Manager is responsible for working with the Clinical Data Management team and other internal project team members to provide data management services for our customers to ensure on time and accurate deliverables. Responsibilities include:

• Providing data management guidance to internal project team members and customers.
• Communicating with internal project team members and customers on all aspects of data management activities performed for a study.
• Authoring data management documents.
• Performing user acceptance testing on data management deliverables.
• Facilitating and verifying data clarifications and data changes.

What you will do:

• Develop and maintain the Data Management Plan (DMP).
• Develop and maintain study-specific Data Cleaning/Reconciliation reports and validation plans.
• Provide weekly data management status updates to the clients and internal Project Managers.
• Work with internal Delivery team to define data management timelines to ensure DM milestones are met.
• Develop other study-specific documentation manuals including but not limited to the Maintenance Guide (MG) as necessary.
• Conduct study-specific trainings with internal Data Coordinators and Data Reviewers prior to release of the Data Management Plan initiatives.
• Adhere to Signant Health Standard Operating Procedures for all data management responsibilities.
• Identify areas of opportunity for improvement in the end to end process of Data Management, driving out waste, increasing productivity and delivering quality.
• Support delivery of improvements in the Data Management process by participating in small group activities, kaizen events and Lean Six Sigma projects when necessary.

Qualifications

• BA/BS degree in a relevant field (Medicine, Statistics, Computer Science) or equivalent work experience.
• Technical aptitudes and ability to complete high quality technical documentation.
• Ability to understand and work with HTML as well as different types of clinical databases.
• Demonstrate extreme attention to detail and organization in all aspects of work.
• Previous project management experience is an advantage.
• Ability to quickly learn and apply new skills, procedures and approaches.
• Demonstrated ability to meet very short deadlines & multi-task in an extremely fast-paced work environment with little direct supervision.
• Proven ability to work both independently and in a team-oriented environment.
• Previously demonstrated proactive and positive approach to tasks and projects overall.
• Proficient in Access, Excel, and other office software technologies and applications.
• Strong verbal and written communication skills.

Requirements

• Collaborate with clients and internal Delivery teams to develop and maintain protocol specific monitoring report specifications.
• Collaborate with clients and internal Data Coordinators and Data Reviewers to generate a study-specific tool for flagging discrepancies between the client IVR/EDC and TrialManager outputs.
• Collaborate with clients and internal Technical Client Services team in order to conduct protocol reviews to identify protocol specific device design and eligibility criteria.
• Collaborate with clients and internal Technical Client Services team to define protocol specific report(s) as necessary.
• Collaborate with internal validation team to define detailed test cases for clinically significant reports.

Benefits

• Collaborative, global environment for career growth.
• Opportunities to learn, take ownership, and drive meaningful innovation.
• Purpose-driven work that advances clinical research and brings new treatments to patients faster.