Lilly is the 10th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 140 years. Across the globe, we are a leader in investing in research and development and we also invest in our employees – in competitive salaries, training and development, and health.
Post : Clinical Trial Registry Specialist
Purpose:
The purpose of the Clinical Trial Registry (CTR) Specialist role is to provide technical and administrative support to meet the needs of the CTR office. The role includes but is not limited to CTR trial tracking through monitoring of global CTR reports and metrics, cross functional communication across geographies and therapeutic areas, tracking and collection of data and Information to ensure compliance. The CTR Specialist establishes appropriate business relationships and will also maintain a working knowledge of CTR timing and processes to achieve accurate and timely registry postings.
Job Responsibilities:
• Contribute to the development, maintenance, and implementation of policies on clinical trial registry database processes and work flows.
• Identify opportunities for process improvements.
• Identify, track and report on clinical trials required for registry postings.
• Work cross functionally with applicable team members and departments across therapeutic areas (e.g.,biostats,medical, clinical trial management), to obtain data required for completion of registry postings).
• Manage access rights to applicable systems as needed
• Provide education and training as required to internal groups.
• Monitor applicable metrics to support overall conformance.
• Create, maintain and utilize technology effectively to manage CTR tracking and reporting processes.
• Identify and access relevant statistical deliverable information needed to ensure that collection is provided for
• Completion of registry records in accordance with regulatory requirements.
• Administratively support CTR systems, processes and workflows.
• Communication/collaboration:
• Communicate to responsible functions the deliverable needs, timelines and deadlines for CTR requirements.
• Conflict resolution and problem solving skills are used to build trust and establish effective collaborations Influence
• Works with other CTR team members to ensure consistent processes are monitored and employed.
• Provides input to deliver innovative solutions, preventing re-occurrence of issues.
• Escalates issues in a timely and appropriate manner.
• Ensures the evaluation (monitoring) of the CTR processes and communicating changes to the processes to the business.
• Shares key learning to drive simplification and replicate best practices.
Candidate Profile
• Associates degree or equivalent required.
• Strong communication skills including written and verbal communication; Demonstrated mastery of English language skills written and spoken.
• Exceptional computer and analytical skills: High proficiency in Microsoft Excel and various databases.
• Demonstrated consistent strong performance in previous positions.
• Demonstrated leadership, self-management & motivational ability.
• Strong Interpersonal skills and the ability to be flexible in varying environments including working across time Zones.
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Additional Skills/Preferences
• Bachelor’s degree preferred
• Impeccable work ethic and positive, solutions-focused attitude.
• Solid ability to drive concurrent projects in a timely manner and with high quality.
• Demonstrated ability to communicate and negotiate solutions to complex technical challenges with cross-functional colleagues, external vendors and customers.
• Demonstrated project management and time management skills including ability to prioritize, multitask and manage multifaceted projects.
• Proven ability to assemble, share and apply key learnings across multiple projects.
• Ability to work well across cultures and time zone
• Ability to work well independently and as part of a team, and ability to assertively marshal the efforts of multiple contributors to projects.
Additional Information:
Location: Bengaluru
Education: Bachelor’s degree
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Regulatory Affairs
Job Code: 39366BR
End Date: 08-Jun-2018
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