Scientific Coding Research Specialist Job at AquSag Technologies (Noida)

Amyloidosis, Medical Affairs Scientist

The MAS role family comprises a variety of medical scientific specialties, such ...

Location

Japan , Tokyo

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Minimum requirement: 4 year university undergraduate degree AND master’s degree in life science, or Pharmacists 4-year university graduates with pharmacist license and master’s degree or above or equivalent life science research experience, or 6–year university graduates with pharmacist license, or Nurses with master’s degree or above, or Veterinarians, or Dentists, or MDs
Preferred: In addition to those who meet the minimum requirements above, the qualifications below are preferred MD (clinical experience, board certification preferred), or PhD in Life Science
Technical Skills: Medical/ pharmaceutical expert knowledge of therapeutic disease area/ products
Ability to communicate appropriately and build good relationship with internal/external stakeholders
Work effectively with teams and across functions by demonstrate Pfizer’s Values & Behaviors and the agility to learn from others
Capable of medical discussion with relevant departments and external HCPs.
A person who understands compliance and relevant laws/regulations in the pharmaceutical industry and advocates the appropriate use of the products.
Can demonstrate appropriate knowledge and understanding of internal organization structure, key stakeholders and strategies
A person who is able to quickly acquire necessary medical/ scientific knowledge and skills though self-learning
Experience: Work experience at functions of: Medical Affairs

Job Responsibility

Demonstrate medical and scientific leadership and expertise
Provide and exchange medical/ scientific information for/from medical institutions (and other related sources) in the assigned area and from stakeholders.
Drive for heightened understanding of the clinical and medical attributes of our products in order to enhance the safe and efficacious use.
Maintain the highest scientific standards during in/ external activities to provide deep medical and scientific expertise.
Contribute to the implementation of local medical strategies and life cycle clinical plans for inline and pipeline medicines / vaccines to address unmet medical needs and fill data gaps.
Make important contributions to decisions of medical strategies for assigned products, in order to ensure safe, proper, and effective use of assigned products.
Contribute to achieving the department/team goals, and/or participate in cross-organizational projects as a core member and provide guidance to deliver the results.
Play an active role in supporting members in the team/organization with the line manager to move towards its goals
Develop and execute the medical plan aligned with the medical strategy to meet unmet medical needs in the assigned product(s) and therapeutic area(s) in collaboration with office medical
Identify unmet medical needs and healthcare disparities in the assigned asset(s) and therapeutic area(s) through medical activities such as advisory board meetings and scientific exchanges with HCPs and other relevant individuals and organizations.

Fulltime

Onc hematology field mas

The MAS role family comprises a variety of medical scientific specialties, such ...

Location

Japan , Tokyo

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

4 year university undergraduate degree AND master’s degree in life science
Pharmacists 4-year university graduates with pharmacist license and master’s degree or above or equivalent life science research experience
6–year university graduates with pharmacist license
Nurses with master’s degree or above
Veterinarians
Dentists
MDs
Medical/ pharmaceutical expert knowledge of therapeutic disease area/ products
Ability to communicate appropriately and build good relationship with internal/external stakeholders
Work effectively with teams and across functions by demonstrate Pfizer’s Values & Behaviors and the agility to learn from others

Job Responsibility

Demonstrate medical and scientific leadership and expertise
Provide and exchange medical/ scientific information for/from medical institutions (and other related sources) in the assigned area and from stakeholders
Drive for heightened understanding of the clinical and medical attributes of our products
Maintain the highest scientific standards during in/ external activities
Contribute to the implementation of local medical strategies and life cycle clinical plans for inline and pipeline medicines / vaccines
Make important contributions to decisions of medical strategies for assigned products
Contribute to achieving the department/team goals, and/or participate in cross-organizational projects
Play an active role in supporting members in the team/organization
Develop and execute the medical plan aligned with the medical strategy
Identify unmet medical needs and healthcare disparities in the assigned asset(s) and therapeutic area(s)

Fulltime

Lung cancer MAS team lead

Acts as a line manager leading a team of MAS. Shapes the local strategy and ensu...

Location

Japan , Tokyo

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Minimum requirement: 4-year university undergraduate degree AND master’s degree in life science, or Pharmacists >4-year university graduates with pharmacist license and master’s degree or equivalent life science research experience, or >6–year university graduates with pharmacist license, or Nurses with a master’s degree, or Veterinarians, or Dentists, or MDs
Preferred: MD (clinical experience, board certification preferred), or PhD in Life Science
Experience in the pharmaceutical industry, preferably as a Medical/Scientific Advisor, MSL, team lead, and/or clinical experience with direct patient care and/or professional experience in the pharmaceutical industry in relevant areas
MA/DJ experience and / or research experience preferred
Scientific publication
Strategic Thinking: Ability to consider the direction of Medical from a mid-to-long-term perspective and formulate strategies as a manager at Pfizer
Communication Skills: Ability to conduct clear and efficient communication, including with other departments, and convey information accurately and logically
Decision-Making Ability: Ability and responsibility to make quick and effective decisions even in situations where there is no clear answer
Leadership: Ability to influence teams and departments and drive them towards achieving organizational goals
Financial Skills: Ability to manage budgets and execute actions reliably and on schedule

Job Responsibility

Acts as a line manager leading a team of MAS
Shapes the local strategy and ensures the delivery of scientific-medical expertise and exchange with KOLs in the assigned therapeutic area
Lead the Pfizer Japan medical scientific point of contact for HCPs, medical societies, regulators, academia and other external stakeholders
Play a central role as a scientific and medical leader who can identify unmet medical needs(UMRs), drive the building and executing medical plans and oversee establishment of clinical evidence
Demonstrate medical and scientific leadership and expertise
Ensure and oversee the highest scientific standards during in / external activities to provide deep medical and scientific expertise
Lead development of local medical plan aligned with global medical plan to address local UMRs and fill data gaps, and manage implementation of local medical strategies and life cycle clinical plans for inline and pipeline medicines / vaccines
Direct and supervise providing and exchanging medical/scientific information for/from medical facilities in the assigned area and external stakeholders and make strategic decisions on medical strategies for assigned products
Drive and monitor heightened understanding of the burden of disease in the assigned therapeutic area and medical attributes of our products to enhance the safe and efficacious use
Lead achievement of department/team goals, and/or manage cross-organizational projects, providing guidance and accountability for results

Fulltime

Python Developer

Take Your Career to the Next Level with Amaris Consulting as a Python Developer!...

Location

Spain

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

+4 years of experience as a Python Developer
Experience in the pharmaceutical or life sciences industry, particularly in digital transformation or data integration projects
Strong proficiency with Python, FastAPI/Flask, and RESTful APIs for backend development
Experience with one or more frontend frameworks (React.js or Angular)
Solid knowledge of cloud platforms (AWS, Azure, or GCP) and version control tools such as Git
Familiarity with containerization technologies (Docker and Kubernetes) and CI/CD pipelines
Proven experience with microservices architecture and web services
Advanced proficiency in English (written and spoken) – mandatory
Strong problem-solving skills and ability to work both independently and as part of a distributed, cross-functional team

Job Responsibility

Integrate mechanistic and data-driven models on the platform by restructuring and migrating original code to align with SMART PD requirements, functionalities, and user interface
Collaborate closely with domain users (i.e., process experts, subject matter experts, and modelling specialists) to gather requirements and translate them into technical solutions
Develop and extend features of SMART PD to significantly improve user adoption, usability, and satisfaction
Write robust, maintainable, well-documented, and production-ready code following best practices
Execute UX research and feedback loops to understand how features impact and improve the experience of scientific and operational users

What we offer

Fast career growth through a personalized development path and regular salary assessments
Upskill with our Technology Academy, Udemy for Business, language classes (English, Spanish, German), webinars, and technical workshops
Take control of your training with a personal annual learning budget and company-sponsored certifications (e.g., AWS, Kubernetes, Docker)
Fully remote work with flexible hours and digital collaboration tools
Excellent social benefits: private health insurance, meal vouchers, transportation allowance, and childcare support
WeCare programme: dedicated support for employees in personal or professional critical situations
International exposure working on high-impact projects in the pharmaceutical and life sciences sectors

Fulltime

Environmental Specialist

A large public water and environmental services agency in Southern California is...

Location

United States , La Verne

Salary:

55.00 - 59.00 USD / Hour

Tucker Parker Smith Group

Expiration Date

Until further notice

Requirements

Bachelor’s degree from an accredited college or university in a related field and four (4) years of relevant experience
OR Two (2) years in an Assistant Environmental Specialist II classification with a similar public agency
OR Master’s degree in a related field and two (2) years of relevant experience
Working knowledge of analytical protocols and scientific terminology used in water and hazardous material testing
Working knowledge of laboratory data analysis and interpretation for environmental investigations
Working knowledge of water treatment and distribution processes and operations
Working knowledge of environmental science theories, methods, and investigative techniques
Working knowledge of federal, state, and local environmental laws, codes, and regulations
Working knowledge of technical research, analysis, and report preparation
Working knowledge of principles, concepts, and techniques of environmental planning at the state, regional, and local government level

Job Responsibility

Coordinate and/or perform wastewater sampling, packaging, chain of custody, and shipping in compliance with permit requirements
Review analytical laboratory data, prepare reports, and assess compliance with wastewater permit requirements
coordinate resampling as needed
Conduct inspections to ensure compliance with environmental program requirements
Participate in program audits and assessment teams
document findings and assist in corrective action development
Document and investigate environmental incidents
Research, analyze, and prepare documentation supporting environmental compliance and process improvements that minimize environmental impacts
Prepare technical reports and deliver presentations as required
Coordinate internal review of documents from external entities and compile comments

Fulltime

Senior Physician, Patient Safety

Join our dynamic Patient Safety team as a Senior Physician where you'll leverage...

Location

United States; Canada , Remote; Alberta

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experience in clinical medicine (general or specialist qualifications) which is expected to be kept up to date
Good knowledge of drug safety and the drug development process
Good knowledge/understanding of medical terminology
Relevant experience in pharmacovigilance/ Drug Safety/ Clinical Practice
3 - 5 years previous experience in pharmacovigilance and/or medical monitoring is required
US Board Certification/board eligibility or regional equivalent for Canada
Bachelor of Medicine, Bachelor of Surgery (MBBS) / Doctor of Medicine (MD)/ Medically qualified from an acknowledged Medical School
Completion of at least basic training in clinical medicine (residency, internship etc.)
Demonstrated success in technical proficiency and scientific creativity
Good presentation and verbal/written communication skills

Job Responsibility

Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and global drug safety regulations and guidelines
Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting
Performing medical review of cases not limited to (including complex and challenging cases requiring expert judgement)), clinical trial, and literature cases including combination products {drug-device}) according to client/Parexel Standard Operating Procedures (SOPs
as applicable) and liaising with the client, as require
Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality
Review appropriateness of medical content in narrative for medical coherence
Assessing seriousness, listedness / expectedness of reported events
Providing medical inputs to case processing team
Raising appropriate follow-up queries for relevant information from the reporter/HCP (Health Care Professional)
Review and verify appropriate selection of adverse events from source documents, assign appropriate Medical Dictionary for Regulatory Activities (MedDRA) code, review narrative

What we offer

Flexible approach to work that meets your personal needs
Work from home
Benefits vary by country
Investment in your professional and personal development

New

Flights Consultant

The Flights Consultant will be responsible for managing and booking all air trav...

Location

United Kingdom

Salary:

28000.00 GBP / Year

Antella Travel Recruitment

Expiration Date

Until further notice

Requirements

Experience booking flights in a travel agency, tour operator, or similar environment
Strong knowledge of GDS systems - Galileo or Amadeus
Excellent knowledge of net fares, seat only, ITX and published fares
Experience in exchanges, refunds, schedule changes, manual fare builds etc
Excellent organisational skills and attention to detail
Strong interpersonal and communication skills
A customer-first mindset with a proactive, solution-oriented attitude

Job Responsibility

Book and manage flight reservations for clients
Coordinate group air blocks as well as individual bookings, depending on customer needs
Managing flight cancellations and schedule changes, ensuring timely rebooking and clear communication to all clients

What we offer

Commission OTE £40,000
Fully remote working within the UK
22 days holiday a year plus bank holidays
Pension scheme
Monday to Friday, 9am to 6pm, Saturdays on a rota basis 10-4 with a day off in lieu
No Sundays or Bank Holidays

Fulltime

New

Evening cleaner

Evening Cleaner Part Time near West County Mall. Housekeeper/General Cleaner nee...

Location

United States , St. Louis

Salary:

14.00 USD / Hour

ServiceMaster by Prince

Expiration Date

Until further notice

Requirements

Must be able and enjoy vacuuming
Must be able and enjoy sweeping
Must be able and enjoy mopping
Must be able and enjoy cleaning bathrooms
Must be able and enjoy emptying trash (sometimes heavy trash) and hauling to the dumpster

Job Responsibility

vacuuming
sweeping
mopping
cleaning bathrooms
emptying trash (sometimes heavy trash) and hauling to the dumpster

What we offer

Competitive Compensation
Paid Time-Off*
Flexible Schedules
No Weekends & Holidays*

Parttime

Scientific Coding Research Specialist

AquSag Technologies

Location:
India , Noida

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 19, 2025

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Scientific Coding Research Specialist

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Location:India , Noida

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Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:December 19, 2025

Looking for more opportunities? Search for other job offers that match your skills and interests.

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Job Posted:
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