Pune, Maharashtra, India
Finance & Banking
Full-Time
Parexel
Overview
Essential Function
The role of Senior Clinical Data Analyst is to independently perform all clinical data cleaning activities on assigned projects, commensurate with experience and/or project role. Responsible for coordinating a moderate to large team or multiple small size protocols as the CDA Coordinator, with minimal to no supervision. Alternatively, take on the role of a CMA/CDA Coordinator on smaller projects.
Key Accountabilities
The role of Senior Clinical Data Analyst is to independently perform all clinical data cleaning activities on assigned projects, commensurate with experience and/or project role. Responsible for coordinating a moderate to large team or multiple small size protocols as the CDA Coordinator, with minimal to no supervision. Alternatively, take on the role of a CMA/CDA Coordinator on smaller projects.
Key Accountabilities
- Assume the ability to meet the requirements of a CDA I and II with a high degree of proficiency and autonomy.
- Act as an independent CDM Coordinator on complex or multiple projects, CMA/CDA.
- Coordinator on smaller projects.
- Manage all phases of data management activities from study start up to database close.
- Direct team members in daily activities.
- Define and monitors metrics and modifies plan accordingly.
- Mentor project team members.
- If required, facilitate cross functional team meetings both internally and externally.
- Actively review and provide feedback on study productivity.
- Recognize out of scope activities and communicates to GRO Lead.
- Represent function in external client meetings and presentations such as investigator meetings and bid defenses as required. May represent Parexel at professional meetings / conferences.
- Keeps manager(s) informed about work progress and any issues to avoid surprises. Requires minimal supervision by Manager.
- Apply knowledge across multiple projects.
- Define study specific processes.
- Identify inconsistencies and inefficiencies in processes and recommends solutions.
- Excellent interpersonal, verbal and written communication skills
- Excellent computer skills including but not limited to the knowledge of Clinical Trial/Data
- Management Systems, PMED, IVRS, MS-Office products such as Excel, Word.
- Sound awareness of all relevant regulations, including GCP
- Posses a thorough understanding of the various tasks related to project initiation, ongoing
- monitoring / processing and lock
- Carefully weighs the priority of project tasks and directs team accordingly
- Understands the strengths and development areas of team members
- Ability to lead a “virtual”, global team as required
- Gives others appropriate latitude to make decisions
- Looks for win-win solutions to solve problems
- Ability to make appropriate decisions in ambiguous situations
- Ability to solve problems by using a logical, systematic, sequential approach
- Communicate and work effectively with clients
- Enlists the support of team members in meetings goals
- Proposes new approaches, methods or technologies
- Anticipates how others will react to situations
- Effective time management in order to meet daily metrics or team objectives
- Shows commitment to and performs consistently high quality work
- Plans and delivers verbal and written communications that persuade the intended audience
- Willing and able to travel as required – local or international
- Bachelor’s degree and / or other medical qualification or relevant DM experience
- Excellent in written and oral English
- Previous relevant working experience preferred, or data management, clinical and / or research experience with solid understanding of clinical trials methodology and terminology.
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