Job as Senior Clinical Data Analyst in Parexel

PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.

Post: Senior Clinical Data Analyst

Job Description:
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.

Candidate Profile:
Previous relevant working experience preferred, or data management, clinical and / or research experience with solid understanding of clinical trials methodology and terminology 4 Yrs. to 7 Yrs of relevant experience

Additional Information:
Experience: 4-7
Location: Andhra Pradesh - Hyderabad
Functional Area: CR
Industry Type: Pharma/ Biotech/Clinical Research
Employment Type: Full Time
Job Type: Regular
End Date: ^20th Feb, 2013
Req Number: pare-10021874