Senior Clinical Data Analyst

ABOUT THIS ROLE

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:

• 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.

Skills:

• 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

Education:

• Bachelor’s degree and / or other medical qualification or relevant DM experience

Language Skills:

• Excellent in written and oral English

Minimum Work Experience:

• Previous relevant working experience preferred, or data management, clinical and / or research experience with solid understanding of clinical trials methodology and terminology.