Vacancy description
Sr. Clinical Data Team Lead in Bangalore, भारत
- RemoteWork from anywhere
- Full-timeStandard weekly hours
- ContractFixed-term or freelance
Bangalore, भारत
JOB DESCRIPTION
Work Schedule
Second Shift (Afternoons)Environmental Conditions
OfficeJob Description
Join Us as a SR Clinical Data Team Lead – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
• Acts as a liaison to the Project Lead and/or client as required and communicates with management regarding all data management (DM) activities within their studies.
• Develops and maintains data management project documentation files; performs independent reviews of data management deliverables following documented CDM guidelines.
• Develops and delivers study specific training for DM project staff.
• Produces project-specific status reports for management, Project Lead and/or clients on a regular basis. Monitors study metrics.
• May participate in business development activities by assisting with bid preparation and/or representing data management at bid defense meetings, where required.
• Assists with project forecasting of hours and identification of resource requirements and identifies potential out of scope activities to Project Lead and management and assists with the Contract Modification process.
• Mentors junior level staff on all associated tasks within a study.
• Assists with the administrative and financial management of allocated projects. Performs all assigned data management activities independently and efficiently, with attention to quality. Education and Experience Requirements:
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities:
• Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, SOPs and client expectations
• Ability to use interactive computer programs
• Good written/ verbal communication skills with a strong command of English language and grammar; good organizational, analytical/problem solving skills and attention to detail
• Ability to work productively with minimal supervision
• Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
• Strong customer focus and excellent interpersonal skills
• Proven flexibility and adaptability
• Ability to work in a team environment and independently as needed
• Ability to train and direct study team
• Ability to set and meet timelines or be able to recognize and schedule changes in response to project demands Working Conditions and Environment:
• Work is performed in an office environment with exposure to electrical office equipment.
• Occasional drives to site locations with occasional travel both domestic and international. Why Join Us? When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference. Apply today to help us deliver tomorrow’s breakthroughs.
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