Researcher

**Description**

**About Norstella**:
At Norstella, our mission is simple: to help our clients bring life-saving therapies to market quicker—and help patients in need.
Founded in 2022, but with history going back to 1939, Norstella unites best-in-class brands to help clients navigate the complexities at each step of the drug development life cycle —and get the right treatments to the right patients at the right time.
Each organization (Citeline, Evaluate, MMIT, Panalgo, The Dedham Group) delivers must-have answers for critical strategic and commercial decision-making. Together, via our market-leading brands, we help our clients:

- Citeline - accelerate the drug development cycle
- Evaluate - bring the right drugs to market
- MMIT - identify barrier to patient access
- Panalgo - turn data into insight faster
- The Dedham Group - think strategically for specialty therapeutics

By combining the efforts of each organization under Norstella, we can offer an even wider breadth of expertise, cutting-edge data solutions and expert advisory services alongside advanced technologies such as real-world data, machine learning and predictive analytics. As one of the largest global pharma intelligence solution providers, Norstella has a footprint across the globe with teams of experts delivering world class solutions in the USA, UK, The Netherlands, Japan, China and India.

**Responsibilities**:
**Business/ Customer**
- Develop a strong command on the business processes, operating procedures as per SOPs and expertise in research and analysis of clinical trials/drug/company profiles/Deals information from public domain in a quick and accurate

manner
- Demonstrate a strong understanding of business models & processes, authoring tool and other tools and extensions used by the team, cultivate robust decision making skills on the process
- Strengthen knowledge of data sourcing and retrieval by exposure to various websites and insights on industry trends, developments and various terms in business research
- Complete all mandatory and aspirational courses on
- time, upskill continuously on domain and behavioral aspects through CTS training programs
- Strongly contribute towards achieving team objectives, displaying enthusiasm, while remaining scientifically and intellectually rigorous
- Work with team leads and Process leads on the assigned tasks and KPIs, should be able to multi-task effortlessly on team assignments
- Display excellent communication skills to interact with teams, client and internal management

**Process**
- Research, verify and validate data and information from various sources, including company websites, trial registries, SEC filings, publications, regulatory sites and journals as per SOP
- Write and update Clinical trial / Drug profile /Deals information based on research findings based on in-house style guidelines and writing style and complete the reports
- Should be able to meet the individual productivity and quality as per assigned target as well as coordinate with other team members/managers on special project requirements from client; Ensure all agreed standards of quality and

accuracy are met at all times
- Manage and coordinate training needs-both fresh and refresher type on domain and process to ensure independent work from the team while maintaining good quality
- Provide process improvement ideas and share best practices with(in) teams, identify and report on process efficiencies identified to the lead/Manager and ensure implementation of the same
- Ensure efficient multi-tasking of all team assignments and take up POC role for tasks on a rotational basis and report progress to leads in timely manner
- Assist the leads in maintaining trackers and team reports, planning and execution of work and overall team task handling

**People**
- Ensure/follow up/assist the team members on timely completion of deliverables, providing training as necessary to ensure data quality; Report to the manager on performance status and any escalations
- Actively participate and contribute to team initiatives: regular team meetings, knowledge sharing sessions, etc.
- Coordinate with other TA teams for work completion
- Handle the training needs of the team and keep a check on team quality

**ADDITIONAL INFORMATION**
**Measurement Criteria**
- Turnaround Timelines (TAT), quality and Productivity
- QA of team, Training Efficiency
- Proper documentation and file management
- Policy and Schedule adherence
- Complete Mandated training programs and Lean Six Sigma

**Requirements**:
**Educational Guidelines**: Graduate/Post Graduate/ Doctorate degree in life sciences/Pharmacy/Medical sciences or equivalent degrees
- Technical Skills - Knowledge of Fundamental Analysis and MS Office Suite
- Sector specific qualification is an added advantage

**Experience Guidelines**
3-4 years of work experience. Experience in Business Research and Analysis/ Secondary data research in life science/healthcare domain is preferred

**Benefi