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Language Research Intern (Indic Languages)

Location: Delhi

Duration: 3 to 6 months (can be extended)

About Chariot

Chariot is a frontier AI research lab based in India that builds foundational AI models. We are one of four teams selected under the IndiaAI Mission to build models from India. We want our models to work as well in Indian languages as the best AI systems work in English.

We're looking for passionate Language Research Interns to own the language infrastructure for one or more Indic languages.

What you will do

You will be responsible for one or more Indic languages that you know well. Your work will include:

• Building test sets to check how well our models perform in your language
• Collecting, cleaning, and improving language datasets, including open-source ones
• Finding words, spellings, and sentence patterns that confuse AI models, and documenting them
• Reviewing model outputs, finding common errors, and working with our researchers to fix them
• Creating language guides and resources that shape how our models are trained and tested

Your work will go directly into our models. When the models improve in your language, that will be because of you.

Who can apply

• You are a native or near-native speaker of at leas

Role Overview:

We are seeking a skilled and experienced Clinical research Manager to lead the clinical study associated activities along with preparing the Clinical Documents efforts for non-active implantable medical devices. This role will also be responsible for guiding the team through design and develop clinical protocols and execute clinical studies (pre-market or post-market studies). The candidate should have extensive experience in clinical evidence generation strategy and scope research topics to provide recommendations on clinical trial strategy. The ideal candidate will bring in-depth knowledge of international medical device clinical research expertise, robust scientific writing capabilities, and demonstrated experience in end-to-end clinical evaluation and evidence generation.

Key Responsibilities:

Clinical Evidence Development:

· Author and maintain high-quality clinical documents including CERs, CEPs, PMCFPs, PMCFRs, PMSP, PSURs, and SSCPs in line with EU MDR and other international standards.

· Conduct thorough risk–benefit analyses and integrate data from preclinical, clinical, and post-market sources.

Cross-functional Collaboration:

· Interface closely with R&D, Clinical Affairs, Marketing, and Regulatory teams to access and identify the necessary preclinical, clinical and technical information.

· Develop clinical and marketing communication tools such a

About the Company

The organisation enables young Indians to pursue high-impact, purpose-driven careers in nation-building. It believes in the power of youth to drive collective change and provides young professionals with the platform to create societal impact. NationBuilding Foundation of India drives interventions to address the most pressing challenges affecting India across priority themes, with sports and health among its focus areas.

About the Preventive Healthcare Vertical

Non-communicable diseases cause the highest number of premature deaths globally. India, too, faces a rising burden of non-communicable and preventable diseases driven by modifiable risk factors. However, the current systemic approach focuses on treatment and management rather than prevention.

The Preventive Healthcare Vertical seeks to shift this paradigm by advancing a science-driven approach to prevention that enables people not only to live longer, but to live healthier for longer. We believe that improving India's health outcomes requires deliberate investment in evidence-based preventive interventions across the life course, with particular emphasis on early-life prevention to reduce the burden of disease later in life.

The vertical is committed to placing healthspan alongside lifespan at the centre of public health thinking. By combining rigorous research, policy engagement, strategic communications, and scala

Applications are invited for the position of Assistant Project Coordinator – (Research)/Senior Researcher on a contractual basis:

Candidates possessing a minimum of 3 years or more of relevant experience will be considered for the position of Assistant Project Coordinator (Research) . However, candidates shortlisted with less than 3 years of relevant experience will be considered for the position of Senior Researcher .

Organisation- Indian Police Foundation

Number of Positions: 1

Tenure- This position is offered initially for 1 year but extendable till the completion of the project. (2027-2028)

Project: Internal Police Reforms Project

Location- Indian Police Foundation HQ, New Delhi (C-8, 8758, Vasant Kunj

New Delhi - 110070) Although the position is in Delhi, the APC- Research/Senior Researcher is expected to travel to various (3 states) both for research as well as project implementation and monitoring.

Qualifications:

Essential:

• Educational Qualification: M.A in Police Sciences/Criminology /Social Work/Public Safety/Law or any other related field. However, candidates with Ph.D. in relevant domains will be preferred.
• R

Designation : Executive – Business Development and Bid Management, Research

Location : Delhi

Educational Qualification : MBA – Marketing, Graduate in Science

Experience: Min 3 yrs in consulting/ services or infrastructure sectors

Remuneration: At par with industry standards

Job Profile:

➢Responsible for business development and marketing of services being offered by Idam Infra and other Idam group companies

➢ Maintaining a database of registrations/empanelments/ accreditations

➢ Maintaining/tracking EOIs, proposals, concept proposals, etc.

➢ Maintaining/updating/coordinating for Case Vignettes and Client Certificates

➢ Coordinating with Practice Leads for tracking business opportunity/weekly report

➢ Coordinating and updating the Corporate brochure/presentation/website updates

➢ Establishing and maintaining contracts with potential clients like multilateral and bilateral agencies, NGOs, etc., to establish rapport and set up meetings for business development.

➢ Preparation/ compilation of detailed proposal/pre-qualification documents for the various business development processes, including competitive bidding/tendering processes.

➢ Assistance in organising the events/ conferences/ workshops/ seminars.

➢ Coordinating with external agencies for publication of articles/ interviews/ participation in conferences/trainin

About the Role

The Executive / Sr. Executive – Electrical (R&D) will contribute to the design, development, testing, and validation of electrical and electronic systems for next-generation air conditioning (AC) products. The role focuses on controller development, PCB design, product performance optimization, and innovation while supporting new product development, cost optimization, and advanced technologies such as IoT in HVAC solutions.

Responsibilities

• Design, develop, and validate electrical and electronic components for controller-based systems

• Develop PCB layouts and perform component-level testing, verification, and validation

• Conduct EMI/EMC testing and support product compliance activities

• Drive cost optimization and localization initiatives through value engineering (VAVE) projects

• Develop IoT-enabled product features and support controller algorithm development

• Investigate product failures through root cause analysis and implement corrective actions

• Prepare and execute software and hardware validation plans for new product development

• Collaborate with Quality and Manufacturing teams during product launch and production support

Qualifications

• 2–5 years of experience in Electrical or Electronics Product Development, R&D, or Product Engineering

• Strong understanding of electronic circuits, controller design, and p

Location: Thane, Mumbai

Employment Type: Full-Time

Open Positions: 2

Key Responsibilities (but not limited to)-

Use & ensure that Standard Operating Procedures (SOPs) concepts, practices in a time sensitive manner for all delegated projects and tasks.

Responsible to ensure the overall success of the designated Clinical operations/ monitoring projects.

Assist PM/APM in the development of study tools and training materials and compliance with standard processes, policies and procedures.

Identify and initiate budget related discussions and recruit investigators in sync with Tech Observer/ sponsor’s SOP’s, GCP and local regulatory regulations.

Assist the Project Manager to develop study management plans and generate tools to facilitate tracking of performance at project level.

Perform on-site/ remote monitoring visits, including site qualification, initiation, monitoring and closeout visits in sync with Tech Observer/ sponsor’s SOP’s, Monitoring plan, GCP and local regulatory regulations. Assist in investigator meetings including preparation, liaison, presentations, problem resolutions, and follow up with site staff as well as vendor and sponsor.

Ensure timely submission of protocol and study related documents for EC/IRB approval.

Maintain TMF and review ISF and other regulatory documentation on an

About Stryde Research

We're a Site Management Organization operating 20+ clinical research sites across Dallas-Fort Worth, Houston, Louisiana, New York, and New Jersey. We serve 1.5M+ patients through 100+ specialized clinics with deep expertise in dermatology, rheumatology, cardiology, and general medicine. We're scaling fast—going from 22 to 35+ team members in 2026—and need someone who can keep our regulatory house in order across multiple sites and studies.

What You'll Actually Do

• Prepare and submit IRB applications, amendments, continuing reviews, and reportable events for multiple sites in US
• Maintain essential documents: 1572s, delegation logs, training logs, investigator CVs, medical licenses, financial disclosures
• Track and manage IRB approvals, renewals, and expiration dates across 15+ active studies
• Coordinate regulatory submissions with sponsors, CROs, and site teams—chase missing documents and keep timelines on track
• Ensure sites maintain current regulatory binders (paper and electronic) that are audit-ready at all times
• Manage protocol deviations: documentation, root cause analysis, CAPA implementation, and sponsor reporting
• Track site training completion and maintain training files per GCP requirements
• Prepare sites for sponsor audits and FDA inspections—conduct regulatory readiness reviews
• Communicate regulatory requirem

We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare professionals to ensure the successful execution of research protocols in accordance with regulatory requirements and ethical standards.

Responsibilities:

1. Coordinate and manage all aspects of clinical research studies from initiation to closeout.
2. Screen, recruit, and enroll eligible participants according to study protocols.
3. Obtain informed consent and ensure compliance with regulatory guidelines and institutional policies.
4. Schedule study visits, perform study assessments, and collect study data accurately and in a timely manner.
5. Communicate effectively with study participants, principal investigators, study sponsors, and other study team members.