Reserach Scientist Iii- Non Medical-ctu Project

6 days ago

Rajarhat Kolkata West Bengal, India Tata Medical Center Full time

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

**Position**

**CTU Project Research Scientist III (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 III (Non-Medical) is a key role responsible for the strategic and operational

management of clinical research projects. This position demands a blend of scientific

understanding, project management expertise, and administrative skills to ensure

successful project delivery.

**Primary Responsibilities**:
Study Design and Planning:
Develop and refine study protocols and designs to ensure scientific rigor and

alignment with research objectives.

Oversee database management and conducting training or activities as per

study requirements.

Analysis Design and Planning:
Design analytical plans and statistical frameworks tailored to the study's

specific needs, ensuring that data collection methods align with intended

analysis strategies.

Reporting and Documentation:
Preparation of all monitoring reports for relevant committees and funding

agency

Organize project meetings to manage progress and timelines

Data analysis and interpretation, writing scientific papers for publications

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.

Project Management inclusive of project planning, workforce management, and

budget oversight.

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.

Conduct training of project staff for database SOPs and other project

meetings.

**Minimum required qualifications/experience**:

- PhD in a relevant field with a minimum of three years of experience post-PhD
- Must have handled a minimum of five projects, as PI or Co-PI./ equivalent
- 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**:

- Significant experience in clinical research management, including overseeing

large-scale projects.
- Strong organizational and leadership skills, with proven ability to manage

multidisciplinary project teams.
- Expertise in regulatory compliance and familiarity with clinical trial protocols

and GCP.
- Excellent budget management and financial oversight capabilities.
- Exceptional communication and interpersonal skills, capable of effectively

managing stakeholder relationships.
- Excellent written and oral communication skills, capable of effectively

presenting research findings and writing complex reports.

**Upper Age Limit: 45**

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

Consolidated Salary: Rs.78000/- + Rs. 21060 (27% HRA) = Rs.99,060 x 12 months

(5% increment on initial emoluments after 2nd year). The successful applicant

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