Ctu Research Scientist I
4 days ago
**Application Closing Date: 15/10/2024**
**Position**
**CTU Project Research Scientist I (Non-Medical)**
**Appointing Organization**
Tata Translational Cancer Research Centre
Tata Medical Centre, Kolkata
**The Tata Medical Centre and the Tata Translational Cancer Research Centre**
The Tata Medical Centre (TMC) is a multispecialty institution for tertiary cancer
care based in New Town, Kolkata. At TMC, clinical and research activities are
integrated to provide state-of-the-art care for patients with cancer. This integration is
enabled by the Tata Translational Cancer Research Centre (TTCRC), the research
arm of TMC. TTCRC is within a dedicated academic space and spread over 3 floors.
At TTCRC, a multidisciplinary team of clinicians, scientists, academics and industry
professionals collaborate to develop a systems medicine approach in cancer research.
This approach is focussed on developing innovative, indigenous, cost-effective and
equitable strategies to improve cancer diagnosis; develop treatments that match
disease characteristics and are adapted to treatment response; and, identify
prognostic and predictive disease biomarkers. These strategies are multi-dimensional
and involve an iterative pathway that include clinical studies, high-throughput
laboratory investigations, computational strategies to integrate, analyse and model
data, hypothesis-based pre-clinical studies and evidence-based translation of findings
to clinical practice. For additional information on work at TTCRC, visit
- childhood-ALL.
We have a dedicated Clinical Trials Unit, which works alongside the clinical team to
run clinical trials and national and International collaborative projects. This post is
for the multicentre study “ICiCLe-ALL-24 - The Indian Collaborative Childhood
Leukaemia Randomised Trial for Children and Adolescents with Acute
Lymphoblastic Leukaemia 2024”.
The Project Research Scientist** **I (Non-Medical) plays a crucial role in shaping the
direction and success of clinical and health services research projects. This position
requires expertise in scientific research, good organizational skills, and the ability to
navigate complex regulatory environments.
**Primary Responsibilities**:
Management of CTSU data team:
The main work of CTSU is capture, management, analysis, and interpretation
on various aspects of the central trial database, data capture, and analysis.
Study Design:
Develop and refine study designs, with special emphasis on statistical plan and
methodology, to ensure scientific rigor and alignment with research
objectives.
Analysis:
Analyse data according to study statistical plan tailored to the study's specific
needs, ensuring that data collection methods align with intended analysis
strategies.
Reporting and Documentation:
Compile comprehensive data reports for relevant committees and funding
agency, that summarize the study progress, challenges encountered, and future
directions.
Data Audit and Compliance:
Data Audits: Perform thorough audits of clinical data to verify accuracy,
completeness, and adherence to the study design and ethical standards.
Leadership:
Lead and motivate a team of data managers and junior analysts to achieve
project goals. Work closely with a multidisciplinary team, including,
statisticians, other researchers, and clinical staff, to ensure that all aspects of
the study are integrated and aligned.
**Minimum Essential Qualifications**:
- First Class Post Graduate Degree, including integrated PG degrees
- Second Class Post Graduate Degree, including integrated PG degrees with
PhD
- For Engineering/IT/CS - First Class Graduate Degree of four years
**Desirable qualifications/experience**:
- Experience in clinical or health research, including expertise in study design
and research methodology. Experience in analysis of large clinical data or
multi-centre clinical studies
- Minimum 3 years of experience in clinical data analysis, statistical analysis of
large datasets, or related field
- Experience in exploratory data analysis, multivariate data analysis, linear,
logistic, Poission regression with diagnostic checking, survival analysis, and
their implementation in R, SAS, Graphpad prism, or other statistical software.
**Necessary qualities**:
- Excellent written and oral communication skills, capable of effectively
presenting research findings and writing complex reports.
- Knowledge of regulatory standards and ethical guidelines pertinent to clinical
research.
- Strong attention to detail and commitment to accuracy.
- Good organizational skills and ability to manage multiple tasks.
**Upper Age Limit: 35**
Duration: Initially for a period of one year extendable for further project period
Consolidated Salary: Rs. 72,800. The position is funded by Indian Council of
Medical research (ICMR). The successful applicant will be managed by and report to
the CTU Manager.
**Enquiries**
Mr Suvasish Mukherjee; Head, Human Resou
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