Reserach Scientist Iii- Non Medical-ctu Project
2 weeks ago
**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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