Research Scientist- Ii Non Medical

3 weeks ago

Rajarhat Kolkata West Bengal, India Tata Medical Center Full time

**Application closing date: 15/05/2024**

**Position**

**CTU Project Research Scientist II (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 “Improving Survival in Childhood Acute Lymphoblastic

Leukemia in India (ISCALL): ICiCLe Implementation Study”.

The Project Research Scientist** **II (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**:
Study Design:
Develop and refine study designs 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 reports for relevant committees and funding agency,

that summarize the study progress, challenges encountered, and future

directions.

Organize project meetings to manage progress and timelines

Preparing manuscripts for scientific communication.

Audit and Compliance:
Site Audits: Conduct regular site visits to ensure compliance with study

protocols and Good Clinical Practice (GCP) guidelines. Address any

deviations or concerns related to study execution.

Data Audits: Perform thorough audits of collected data to verify accuracy,

completeness, and adherence to the study design and ethical standards.

Collaboration and Leadership:
Team Collaboration: Work closely with a multidisciplinary team, including

data managers, statisticians, other researchers, and clinical staff, to ensure that

all aspects of the study are integrated and aligned.

**Minimum required qualifications/experience**:

- First class post-graduate degree, including integrated PG degrees, with three

years’ experience or PhD
- Desirable: Experience in clinical or health services research, including

expertise in study design and research methodology. Experience in

conducting/managing operational feasibility studies

**Necessary qualities**:

- Excellent written and oral communication skills, capable of effectively

presenting research findings and writing complex reports.
- Demonstrated ability to lead and manage research projects, including

coordination of interdisciplinary teams.
- 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: 40**

Duration: Initially for a period of one year extendable for further project period

Consolidated Salary: Rs 90,000. The position is funded by Indian Council of

Medical research (ICMR). The successful applicant will be managed by and report to

the CTU Administrator.

**Enquiries**

Mr Suvasish Mukherjee;
Head, Human Resources;
Tata Medical Center; 14 Major Arterial Road (East-West);
Newtown, Rajarhat; Kolkata 700 160

For informal enquiries,

XXXX

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