Requirement Analyst ( Clinical Research Projects) by PAREXEL International (India) Pvt. Ltd. , Hyderabad B8

Job Description

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JD:Requirement Analyst

Key Accountabilities:

• Develop and provide leadership in developing requirements. This includes requirements elicitation, requirements analysis and negotiation, requirements validation, and requirements management.
• Develop requirement specifications in support of 1 or more project efforts using available requirements tools and templates.
• Development and storage of templates for use in support of project efforts.
• Ensure that all project requirements have been stated unambiguously; and that inconsistencies, omissions, and errors have been detected and corrected.
• Help the project team to identify, control, and track requirements and changes to requirements at any time as the project proceeds.
• Participate in documentation reviews.
• Drive consistency within projects, products and within clients.
• Promote efficiency, quality and consistency in requirements design process
• Use initiative and innovation to remedy problems with limited supervision Ensure compliance with SOPs and other relevant regulatory agency regulations Maintain a positive, results oriented work environment, building partnerships and modeling teamwork, communicating to the team  n an open, balanced and objective manner Customer Service
• Proactively communicate with the client providing regular and timely updates.
• Understand and appreciate the clients business need.
• Able to translate often complex technical and/or requirement descriptions into language that can be understood by clients to aid in their decision making and understanding of project functionality.

Business skills

• Provide business intelligence in respect of new service and product development opportunities.
• Collaborate with key account directors (and other relationship stakeholders) to highlight areas of client opportunity or relationship concerns.
• Provide operational support for bid defense meetings

Job Qualifications

• 5 to 8 years of relevant work experience preferred, including but not limited to; working in a customer service related environment; working with IVR or RTSM; working in a clinical trials environment Experience in collecting, organizing and analyzing requirements preferred.
• Experience in a clinical or technical operations environment preferred.
• Familiarity with regulatory agency regulations such as FDA 21 CFR Part 11 and GxP helpful Preferably 1 or more years client facing experience in a PM role or equivalent
• Excellent interpersonal, verbal and written communication skills.
• Client focused approach to work.
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload Interviewing skills, to talk with stakeholders in individual and group settings about their needs.
• Questioning skills, to frame questions in order to surface key requirements detail.
• Listening skills, to understand and absorb input from all stakeholders.
• Critical thinking to evaluate information gathered from multiple sources, reconcile conflicts, and decompose high-level information into details.
• Facilitation and collaboration skills, to lead constructive meetings between internal and external teams.
• Organizational skills, demonstrating attention to detail, to work in a dynamic and changing environment with an extensive collection of  internal and external information gathered during the requirements analysis process.
• Modeling skills, to represent requirements where necessary in tabular and graphical forms in order to augment textual descriptions.
• A flexible attitude with respect to work assignments and new learning.
• Ability to work in a matrix environment and to value the importance of teamwork.
• Proficient in Microsoft Office including Word, PowerPoint, Excel and Visio.

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