medical research scientist

Institute of Obstetrics and Gynaecology, MMC.

The Project Research Scientist II (Medical) will be responsible for:&middot; Providing support to research nurses in recruitment of study subjects anddata collection.&middot; Ensuring data accuracy and completion (both manual and digital)&middot; Entering data into database, manage and maintain effective record keeping data&middot; Providing support to project office operations performing a variety ofstandard administrative duties including typing of official documentsensuring high quality and accuracy of work&middot; Keeping track of project with update reports&middot; Any additional work related to current project and other related projects asinstructed by the PIEssential qualifications and experienceMBBS / BVSc / BDS with three years&rsquo; post qualification experienceOrMBBS / BVSc / BDS + Post Graduate Degree (MD/MVSc./MDS/MPH) or anyequivalent degree, including integrated PG degreesOrMBBS/BVSc/ BDS with PhDDesirable qualifications and experience1. Postgraduate degree or diploma in clinical trial management2. Experience as a project scientist in at least one research project involvingfunding agencies like ICMR, DBT, DST, SERB, Welcome Trust, GatesFoundation, etcSkills<ul><li>Proficient knowledge of data, data dictionary, database, research data</li><li>workflow, etc.</li><li>Basics of biomedical research including informed consent process</li><li>Well versed in recording the data</li><li>Excellent reading comprehension and strong written as well as verbal</li><li>communication skills, including good command of English is required</li><li>Good understanding of needs for project and job responsibilities</li><li>Proficiency in using computers (Windows and mac OS), internet,</li><li>troubleshooting, using cloud storage of various types. Good organizational</li><li>behavior and problem-solving skills</li><li>Ability to establish and maintain effective working relationships with co-</li><li>workers and investigators.</li></ul><ul><li>Schedule of selection (subject to change)</li><li>Last date of receiving applications: 27 Dec 2025 at 5 PM.</li><li>Screening test/Interview (Interaction with shortlisted candidates) on 29 Dec 2025.</li></ul>Job Type: Contractual / Temporary Contract length: 36 monthsPay: ₹960,000.00 - ₹1,248,000.00 per yearWork Location: In person

Research Scientist II (Medical)

NTENT

<div><div>Research Scientist</div>
<div></div><div>Position: Full time</div>
<div>Location: Carlsbad office</div>
<div></div><div>About Us:</div>
<div>NTENT provides a Platform-as-a-Service (PaaS), allowing industry partners to customize, localize and integrate Voice Assistant and Search technologies directly into their business-to-consumer offerings. NTENT utilizes a machine learning algorithmic approach to comprehend massive amounts of information across the web. Through the company&rsquo;s proprietary search engine, ontology and knowledge graph, NTENT makes it easier to decipher meaning, surfacing the most relevant answers, results, content and ads, via conversational interfaces or text. 
 
We are a unique group of brilliant minds intent on discovering, learning and building. We work in a vibrant atmosphere, with an emphasis on personal and professional development. This is an opportunity to tackle complex problems usually reserved for a handful of large companies in the search industry.</div>
<div> 
About the Opportunity: 
We are a dynamic company looking for our next great hire to join our team in Carlsbad, California.</div>
<div></div><div>We are looking for a Research Scientist to join our team and drive research and development efforts for our News Platform and systems that evaluate the quality of documents and detect misinformation.</div> 
<div></div>
<div></div><div>Duties and Responsibilities:</div>
<ul><li>Partner with product managers, machine learning scientists and engineers to formalize appropriate research questions that are relevant to our News Platform.</li>
<li>Conduct independent research, perform extensive literature reviews, sort through prior published work to find potential solutions.</li>
<li>Design experiments and lead data collection efforts.</li>
<li>Work with large amounts of text data and leverage statistical and machine learning methods.</li>
<li>Communicate and transfer solutions to production together with scientists and engineers.</li>
<li>Communicate ideas, methods, opportunities, and results to cross functional partners.</li></ul> 
<div></div><div>Skills and Qualifications:</div>
<div></div><ul><li>Graduate degree (PhD preferred) in Computer Science, Linguistics, Statistics, Computational Social Sciences or other quantitative field.</li>
<li>3+ years of professional experience or equivalent experience in a research lab. Recent PhD graduates are especially encouraged.</li>
<li>Broad experience on with various applications of NLP (part-of-speech tagging, dependency parsing, entity recognition and extraction etc.)</li>
<li>Broad experience in machine learning and statistical methods, in at least one of the following areas: experimental design, causal inference, machine learning, reinforcement learning, deep learning.</li>
<li>End-to-end experience in research projects, including study design, simulation/testing, data cleaning, data analysis, and reporting.</li>
<li>Proficient with Python or R.</li>
<li>Experience with Spark, PySpark.</li>
<li>Exceptional written, verbal, and visual communication.</li>
</ul>
<div></div><div>The following experience is a plus:</div>
<ul><li>Experience in the news domain (fact checking, detecting misinformation etc.) and knowledge of journalistic principles highly desired.</li>
<li>Experience in computational journalism highly desired.</li>
<li>Publication track record is a big plus!</li>
</ul>
<div></div><div>The ideal candidate will be self-motivated, possess excellent communication skills (both oral and written) and be able to work independently. A keen interest in various aspects of language processing is essential in our multi-disciplinary team.</div>
<div></div><div>We offer a full comprehensive benefits package including medical, dental and vision. Employees receive a generous time off (PTO) plan and 13 holidays per year. We also offer 401(k) benefits, long term disability benefits and life insurance.</div></div><div></div>

Research Scientist

HEOR Scientist - Pneumococcal Vaccines Location: RemoteContract Type: TemporaryRate: £650-800 per day approx. (Umbrella) SRG are supporting a leading global pharmaceutical company with their search for an HEOR Scientist supporting Pneumococcal Vaccines. This will be an initial 9 month contract and the role is predominantly remote based. Reporting to the Global RWE & Health Outcomes Research Lead, you'll play a key role in designing and delivering impactful real-world evidence (RWE) studies that inform strategic decisions and support global market access. Key Responsibilities <ul> <li>Design and execute multiple RWE studies, managing timelines, deliverables, and budgets.</li><li>Ensure quality and compliance across study documentation including protocols, analysis plans, and publications.</li><li>Translate strategic evidence needs into innovative study concepts and protocols.</li><li>Advise internal and external stakeholders on scientific design and data sources.</li><li>Build strong cross-functional relationships across medical, market access, and commercial teams.</li><li>Engage with external thought leaders to ensure robust and credible research approaches.</li></ul> Requirements & Experience <ul> <li>MSc or equivalent in health economics, epidemiology, pharmacy, or life sciences.</li><li>1-3 years' experience in the pharmaceutical industry, ideally within a multinational setting.</li><li>Proven ability to manage projects and budgets in a matrix environment.</li><li>Experience with RWE study designs and HTA/reimbursement evidence generation.</li><li>Experience with Pneumococcal Vaccines would be a major advantage - Vaccines in general or Immunology also useful experience</li><li>Strong communication skills to translate complex data for diverse audiences.</li><li>Knowledge of global healthcare systems and payer decision-making processes.</li></ul> Preferred: PhD/PharmD, launch experience, and direct payer engagement. To Apply If you are interested and want to find out more about this role, please click to apply or contact Theo Charles to discuss further. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

HEOR Scientist - Vaccines

Research Foundation for Mental Hygiene, Inc.

<div>
 
 Job Title:
 
 Research Scientist III
 
 
 
 Grade:
 
 25
 
 
 
 Salary:
 
 $88,938 -$98,938
 
 
 
 Location:
 
 Albany, New York
 
 
 The Research Foundation for Mental Hygiene is seeking a qualified candidate to fill a full-time Research Scientist III position located within the New York State Office of Mental Health.
 
 
 
 Duties And Responsibilities
 
 
 
 <ul>
 <li>
 Explore trends and causes of incompetent-to-stand-trial orders; evaluate programs for and understand success of those adjudicated not responsible by reason of mental disease or defect;
 </li>
 <li>
 Assess outcomes related to patients discharged from orders; evaluate the Serious Mental Illness Violence risk program; request and coordinate the receipt of criminal history data for program evaluation;
 </li>
 <li>
 Evaluate the Resident Rehabilitation Units; assist the Jail Diversion Center with evaluations of local diversion programs; coordinate and conduct an evaluation of Crisis Intervention Teams and Mobile Access Program;
 </li>
 <li>
 Prepare research reports on best practices related to various populations and programs, and present the contents of those reports virtually and in-person;
 </li>
 <li>
 Assess the statistical methods and procedures used to determine best practices to ensure validity, applicability, efficiency and accuracy; perform descriptive and multivariate statistical analyses of data;
 </li>
 <li>
 Analyze and interpret statistical data; prepare tables, graphs, fact sheets and written reports summarizing research results.
 
 
 </li>
 </ul>
 
 Required Skills
 
 
 
 <ul>
 <li>
 Ability to conceptualize and execute a complete quantitative analysis;
 </li>
 <li>
 Experience conducting reviews of scientific literature, scientific writing, publications and presentations;
 </li>
 <li>
 Experience with the mental health systems and criminal justice programs;
 </li>
 <li>
 Proficiency in the use of SPSS or other statistical analysis software and standard Microsoft applications;
 </li>
 <li>
 Strong relational and multidimensional data modeling skills;
 </li>
 <li>
 Experience structuring and executing data extractions from data management systems;
 </li>
 <li>
 Experience using Tableau and SQL.
 
 
 </li>
 </ul>
 
 Minimum Qualifications
 
 
 
 <ul>
 <li>
 Master's degree in economics, Psychology, Criminal Justice, Public Health, or a related field; and three years of experience or Ph.D. in an appropriate field and 2 years of experience.
 
 
 </li>
 </ul>
 
 Work Location:
 
 75 New Scotland Avenue, Albany, NY 12208
 
 
 
 To Apply:
 
 Submit an application through our website at https://rfmh.applicantpro.com/jobs/. Please note only applications submitted through our website will be considered.
 
 
 The Mission of the Research Foundation for Mental Hygiene, Inc. (RFMH) is to promote the mental health of all New Yorkers, with a focus on providing hope and supporting recovery for adults with serious mental illness and children with serious emotional disturbances. Applicants with lived mental health experience are encouraged to apply. RFMH is deeply committed to supporting underserved individuals, organizations, and communities. To this end, RFMH is focused on implementing activities and initiatives to reduce disparities in access, quality, and treatment outcomes for underserved populations. A critical component of these efforts is ensuring that RFMH is a diverse and inclusive workplace where all employees' unique attributes and skills are valued and utilized to support the mission of the Agency. RFMH is an equal opportunity/affirmative action employer.
 
 
 The Research Foundation is a private not-for-profit corporation and is not an agency or instrumentality of the State of New York. Employees of the Research Foundation are not state employees, do not participate in any state retirement system, and do not receive state fringe benefits. Excellent Benefits Package. Affirmative Action/Equal Opportunity Employer - Disabled/Veteran, 41 CFR 60-741.5(a) and 41 CFR 60-300.5(a) compliant.
 
 
 Salary: $88938 - $98938 per year
 
 
 
 Job Posted by ApplicantPro
 
</div>

Research Scientist III

St. John's Research Institute

<div><div>Brief Description about the Project
The Intensive Care Unit (ICU) is designed to support life during critical illness; however, in patients with advanced or terminal conditions, continued or escalated intensive interventions may offer limited benefit and instead prolong suffering for patients and families.
In India, organ-based protocols and parameter-based interventions in ICUs, along with the pro-life sociocultural expectations, gaps in prognostication communication-skills, defensive medical practices, and ambiguity around medico-legal frameworks, have all contributed to institution of non-beneficial disproportionate treatments in the terminally ill. Although there are guidelines developed jointly by the Indian Society of Critical Care Medicine and the Indian Association of Palliative Care, their implementation in routine ICU approach and practices remain inadequate. To address these gaps, the Multifaceted Comprehensive Appropriate Care Package (MCACP) is being developed as a structured, evidence-based framework integrating palliative care principles into ICU workflows.
This study aims to develop and pilot the MCACP in ICU setting to, use timely triggers, refine implementation strategies, identify facilitators and barriers, and assess preliminary outcomes, including quality of dying, family satisfaction, and care de-escalation practices. Focus will be on developing methods for appropriate and timely integration of structured palliative care to maintain care-continuum, and quality of life up to, and including the end-of-life period.
Project Research Scientist &ndash; III (Non-Medical) (Implementation of the project in the ICU)
No. of Vacancy: one
Project start date:02/02/2026
Duration of the Project:2 years
Essential Qualification:
<ul><li>Master with research experience or PhD degree in Psychology, Public Health.</li>
<li>Working knowledge of Kannada and Microsoft 365 Office Suite.</li>
<li>Certified in Good Clinical Practice.</li>
<li>Experience in qualitative and quantitative research</li>
</ul>
Minimum Skills expected
<ul><li>Skills to interview, record and transcribe interviews</li>
<li>Conduct Focused Group Discussion</li>
<li>Ability to use distress protocol as needed</li>
<li>Familiarity with implementation science frameworks (e.g., CFIR, NPT)</li>
<li>Research Rigour, and Attention to Details</li>
<li>Inclusive, system and solution- based approach</li>
</ul>
Experience: Minimum 5 years
Preferred Language:English, Kannada and Hindi
Location: Bangalore
Salary: Rs.1,01,400 /- per month
Age Limit: 45 Years
Roles &amp; Responsibilities:
<ul><li>Lead data management and quality control processes for the research projects assigned by the PI.</li>
<li>Prepare and use frameworks such as CFIR (Consolidated Framework for Implementation Research) and NPT (Normalization Process Theory</li>
<li>Conduct qualitative interviews and analyze implementation outcomes.</li>
<li>Facilitate the systematic documentation of intervention fidelity using tools (TIDieR -Template for Intervention Description and Replication), and other questionnaires as a part of research studies.</li>
<li>Oversee the execution of MCACP program, and prepare evaluation reports for the site</li>
<li>Conduct midline and endline analyses to inform programmatic and policy recommendations</li>
<li>Coordinate multi-disciplinary review meetings, and within institution-stakeholders, including patient-family</li>
<li>Contribute to developing suitable methods to ensure proportionate care</li>
<li>Act as an independent assessor to ensure objectivity and rigor in evaluating implementation fidelity, ethical compliance, and the contextual adaptability of the MCACP intervention. The complexity and multidimensional nature of this implementation research necessitate having an independent evaluator at each site who is separate from the implementing team.</li>
<li>Collaborate with the central research team and technical partners to incorporate local findings into cross-site synthesis towards development of a technical resource hub.</li>
<li>Play a frontline role in delivering interventions at ICU sites, and beyond, ensuring care-continuum for the patient.
</li><li>Contribute to conducting staff-training</li>
<li>Monitor fidelity, supervise, enforce research rigor, and maintain quality assurance across the clinical and operational dimensions of the project</li>
<li>Major role in drafting, reviewing, revising the manuscripts ensuing out of the institution-based research projects, until publication.</li>
</ul>
Interested candidates may send their Resume to:
The Principal Investigator
ICMR MCACP Implementation Research Project
SJRI
To Apply: E-mail cover letter and curriculum vitae with 3 references (names and email addresses / phone numbers) by on or before 15th January, 2026 hod.ppalliative@stjohns.in and cc to hr@sjri.res.in</div></div>

Project Research Scientist – III (Non-Medical) (Implementation)-ICMR MCACP Project

ONE NUCLEUS

3 Month Contract Near Cambridge UK Scientist / Bioanalytics, PK assays, MSD Candidates will need to be available to start quickly, be able to be based in Cambridge, have right to work in the UK and have experience with the above techniques. Some training could be given to certain areas lacking. Please send CV's direct via LinkedIn to Louisa Hodgson in the first instance and for suitable candidates she will organise a call to discuss more insight. This role will support a leader in a time of need, so if you can confidently help us with the above then we would welcome hearing from you with your CV. Candidates without the immediate right to work in the UK unfortunately cannot be considered.

Scientist / Bioanalytics, PK assays, MSD

ECLARO

<div>
 
 Job Number: 25-05682
 
 
 
 Use your skills where innovative technology solutions begin. ECLARO is looking for a
 
 Research Scientist
 
 for our client in
 
 Piscataway, NJ.
 
 
 
 ECLARO&rsquo;s client is a leading consumer products company with a global presence. If you&rsquo;re up to the challenge, then take a chance at this rewarding opportunity!
 
 
 
 Position Overview:
 
 
 
 <ul>
 <li>
 Perform appropriate Lab practices and procedures for making product formulation and testing of products.
 </li>
 <li>
 Follow product stability protocols.
 </li>
 <li>
 Maintain, monitor, validate and calibrate lab equipment, as necessary.
 </li>
 <li>
 Prepare reports, collect data analysis, and communicate progress and completion of tests to leadership.
 </li>
 <li>
 Maintain good record keeping habits.
 
 
 </li>
 </ul>
 
 Pay Rate:
 
 $50.00/Hour
 
 
 
 Responsibilities:
 
 
 
 <ul>
 <li>
 Lead the development and implementation of new toothpaste formulas for North America - under the hello and Tom's of Maine brands.
 </li>
 <li>
 Be the R&amp;D point of contact for commercial teams for hello and Tom's key innovation.
 </li>
 <li>
 Lead experimental designs to help identity launch formulations and production processes.
 </li>
 <li>
 Make lab and pilot batches of formulations for stability testing and customer sampling.
 </li>
 <li>
 Support Pilot Plant batches by preparing batch sheets, requesting raw materials, pre-weighing materials and batch execution.
 </li>
 <li>
 Support plant trial batches at various North America locations as needed.
 </li>
 <li>
 Manage multiple stability studies at the lab, pilot and plant scale, working with support groups (analytical, flavor, micro, etc.) to deliver samples and follow up on results.
 </li>
 <li>
 Create/maintain all required R&amp;D documentation to ensure flawless, high quality commercialization.
 </li>
 <li>
 This may include R&amp;D project timelines, formula databases, tech transfer checklists, proof of claims documents, registration documents, NODs, change control documents and technical justifications.
 </li>
 <li>
 Manage independent projects and collaborate with cross-functional teams, leveraging diverse perspectives to achieve key project goals and influence beyond your network
 </li>
 <li>
 Create and maintain all required documentation under GMP/GLP per FDA/ICH guidelines as required.
 </li>
 <li>
 Validate new raw material suppliers and packaging as required.
 </li>
 <li>
 Maintain a clean and organized working environment.
 </li>
 <li>
 Work on multiple tasks with changing priorities.
 </li>
 <li>
 Make day-to-day recommendations and escalate issues regarding formula development.
 </li>
 <li>
 Stay abreast of supplier and competitor's new developments.
 </li>
 <li>
 Abide by and follow all company standard operating procedures (SOPs) including those for product development, regulatory and safety.
 </li>
 <li>
 Deliver effective presentations of technical data and project status.
 
 
 </li>
 </ul>
 
 Required Qualifications:
 
 
 
 <ul>
 <li>
 4+ years of experience developing and/or implementing consumer products.
 </li>
 <li>
 Experience scaling up formulations from the lab through pilot or manufacturing scale.
 </li>
 <li>
 Technical understanding of related chemistry and science (for example: active deliveries, emulsions, surfactants, rheology, liquid chemistry)
 </li>
 <li>
 Strong knowledge of ingredient chemistry to be able to understand how the interdependencies and interactions of raw material components affect formulation and process performance
 </li>
 <li>
 Able to multi-task and coordinate various simultaneous projects
 </li>
 <li>
 Strong oral and written communication skills
 </li>
 <li>
 Self-motivated but able to work well within a team environment
 </li>
 <li>
 Knowledge of cGMP /GMP and GLP
 </li>
 <li>
 Excellent computer skills (MS Office, Google suite, SAP, etc.)
 </li>
 <li>
 Previous laboratory experience preferred.
 </li>
 <li>
 Must have hands-on experience with laboratory instruments.
 </li>
 <li>
 Must be able to learn new procedures in a short period of time.
 </li>
 <li>
 Must be able to follow SOPs and obtain reliable and accurate data.
 </li>
 <li>
 Must be able to document data consistently and accurately.
 </li>
 <li>
 Must be able to perform routine tasks daily.
 
 
 </li>
 </ul>
 
 Preferred Qualifications:
 
 
 
 <ul>
 <li>
 Knowledge of equipment and procedures for making oral care formulations.
 </li>
 <li>
 Experience running stability studies for OTC/Drug products.
 </li>
 <li>
 Experience &amp; understanding of producing formulations at the manufacturing scale.
 </li>
 <li>
 Experience with claim substantiation.
 </li>
 <li>
 Strong project planning and management experience.
 </li>
 <li>
 Knowledge of Regulatory environment in North America and across the globe.
 </li>
 <li>
 Knowledge of ICH/FDA guidelines for stability and testing of new drug products.
 
 
 </li>
 </ul>
 
 If hired, you will enjoy the following ECLARO Benefits:
 
 
 
 <ul>
 <li>
 401k Retirement Savings Plan administered by Merrill Lynch
 </li>
 <li>
 Commuter Check Pretax Commuter Benefits
 </li>
 <li>
 Eligibility to purchase Medical, Dental &amp; Vision Insurance through ECLARO
 
 
 </li>
 </ul>
 If interested, you may contact:
 
 
 
 Carlo Flores
 
 
 
 
 Carlo.Flores@eclaro.com
 
 
 
 
 6466952934
 
 
 
 
 Carlo Flores | LinkedIn
 
 
 
 
 Equal Opportunity Employer:
 
 ECLARO values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status, in compliance with all applicable laws.
</div>

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10000 medical research scientist jobs NEAR_ME

Research Scientist II (Medical)

Research Scientist

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Research Scientist III

Project Research Scientist – III (Non-Medical) (Implementation)-ICMR MCACP Project

Scientist / Bioanalytics, PK assays, MSD

Research Scientist