Scientific Coding Research Specialist Job at AquSag Technologies (Noida)

Scientific Coding Research Specialist

We are hiring highly analytical and computationally proficient researchers acros...

Location

India , Noida

Salary:

Not provided

AquSag Technologies

Expiration Date

Until further notice

Requirements

PhD or PhD candidate in Computational Physics
At least one peer-reviewed publication
Advanced proficiency in Python for scientific coding
PhD or PhD candidate in Computational Biology or Bioinformatics
At least one peer-reviewed publication
Advanced Python skills for modelling or biological computation
PhD or PhD candidate in Computational Mathematics
At least one peer-reviewed publication
Advanced Python skills for numerical methods or algorithmic computation
PhD or PhD candidate in Computational Chemistry

Job Responsibility

Develop original, research-grade or graduate-level scientific problems in your domain
Use Python for scientific coding, modelling, simulation or analytical computation
Define problem categories, secondary tags and difficulty levels clearly
Solve all formulated problems rigorously, ensuring methodological precision, reliability and coherent reasoning
Participate in two-tier review cycles to evaluate accuracy of problems and solutions
Review peer submissions with a focus on scientific correctness and internal consistency
Incorporate feedback promptly and refine content to maintain high quality standards
Work closely with reviewers and team leads to uphold overall technical excellence

Principal Physician, Patient Safety

Location

India

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
Expertise in drug safety and the drug development process
Demonstrated success in technical proficiency and scientific creativity
Ability to work on complex problems requiring in-depth evaluation
Ability to exercise judgment within broadly defined practices and policies
Good presentation and verbal/written communication skills
Good interpersonal skills
Client focused approach to work
Demonstrated ability to balance technical expert responsibilities with people management duties when assigned
Computer proficiency, ability to work with web-based applications and familiarity with the Windows operating system and Microsoft Office apps

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
Communicating and discussing issues related to review process with Line Manager/Project Leader/Designee
Interacting with internal and external stakeholders for resolving issues
Attending and/or presenting at client/cross functional meetings along with other stakeholders
Working as Subject Matter Experts (SMEs)
Assisting the Project Lead/Functional Lead for audits and inspections, Act as a Subject Matter Expert during Audits/inspections
Provides inputs for process improvements
Works closely with Project Lead/Functional Lead for process co-ordination and to ensure meeting all Key Performance Indicators (KPIs) for the process
Function as pharmacovigilance representative/safety scientist

Fulltime

Deputy Laboratory Manager

We are seeking an experienced and motivated Deputy Laboratory Manager to support...

Location

United Kingdom , Northampton

Salary:

54500.00 GBP / Year

CARE Fertility

Expiration Date

Until further notice

Requirements

BSc (minimum 2:1 or equivalent) in a relevant life science subject
HCPC registration as a Clinical Scientist
Proven experience in a reproductive science leadership or senior embryology role
Competent in ICSI, oocyte vitrification and embryo biopsy
Experience training and supervising junior scientific staff
Strong understanding of quality management systems and laboratory governance
Excellent organisational, communication and decision-making skills
RCPath Part I/II or HSST (or working towards)
Leadership or management qualification
Experience working within an HFEA-licensed environment

Job Responsibility

Undertake all routine embryology laboratory duties in line with SOPs, COSHH requirements and the HFEA Code of Practice
Maintain high standards of patient care, traceability, data integrity and laboratory safety
Oversee equipment maintenance, stock control and reagent management
Support effective cryostorage management in collaboration with the central cryomanagement team
Participate in weekend, on-call and flexible working patterns as required
Support and deputise for the Laboratory Manager, including providing laboratory oversight in their absence
Supervise, train and mentor scientific and support staff, acting as a role model for professional practice
Allocate workloads, maintain safe staffing levels and contribute to workforce planning
Chair team meetings and contribute to clinic and senior management discussions
Support performance management, appraisals, induction and staff development

What we offer

33 days' annual leave (including public holidays)
Pension scheme
Life assurance
A range of other benefits, including retail discounts and access to our wellbeing hub

Fulltime

Clinical Innovation Specialist

We are on a mission to ensure everyone has access to medical expertise, no matte...

Location

Denmark , København

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

MD with some postgraduate clinical experience
A PhD demonstrating high quality research output involving significant data manipulation and analysis
The ability to move seamlessly between clinical reasoning and quantitative thinking
A genuine love for data, statistics and scientific inquiry, not just as tools but as a way of thinking
Curiosity about how things work at a technical level, and humility to learn from engineers and colleagues with very different backgrounds
Comfort with ambiguity: you can define problems, propose methods, and move forward without predefined answers
Openness to working with agentic coding as a core workflow—you don’t need to be an expert on day one, but curiosity and a genuine desire to learn

Job Responsibility

Collaborate with our engineers to develop and refine evaluation approaches for clinical AI, both in the backend and in pragmatic evaluations of the final product
Run experiments and build prototypes: you will test ideas hands-on and tinker with their settings and architecture
Bring statistical and methodological rigour to product decisions, partner discussions, and regulatory inputs
Critically assess relevant clinical literature and translate insights into product improvements
Represent Corti's scientific approach in selected partner and customer engagements
Translate qualitative clinical observations and feedback into measurable, testable evaluation criteria
Close the loop between clinician experience and system performance
Contribute to prompt and workflow improvements tailored to customer and partner needs
Produce high-quality scientific output (case studies, white papers, regulatory contributions, conference presence) that builds Corti's credibility with clinical decision-makers, procurement, and regulators
Contribute to clear, compelling artifacts that that communicate our methodology and evidence base

Fulltime

Associate Process Engineer

The Associate Process Engineer is responsible for utilizing existing process pro...

Location

United Arab Emirates , Dubai

Salary:

Not provided

McDermott

Expiration Date

Until further notice

Requirements

Bachelor’s Degree or Master’s Degree in Engineering
0-3 years of experience in oil and gas
Learning the content and application of standards, codes, and guidelines as applicable
Learning design techniques and analysis methods
Preferably Registered Engineer in Training (EIT) or member of a professional engineering society as applicable
Is familiar with process design and unit operations
Is current with the latest scientific and engineering methods

Job Responsibility

Perform detailed design engineering, analysis, and calculations on basic engineering tasks
Apply knowledge and skills to complete routine assignments under close supervision and mentoring
Prepare clear and accurate detailed design calculations and analyses including design reports and procedures
Organize own work to meet deadlines set by others
Clearly communicate information, asking questions, and checking for understanding
Gain understanding of the project scope of work, specifications, schedule, and all inter-discipline requirements
Develop basic knowledge of MDR's business units
Develop a basic understanding of MDR's business and the customers it serves
Develop basic knowledge of the interactions between the departments
Develop advanced skills in the use of standard productivity tools such as Microsoft Word, Excel, and PowerPoint

Fulltime

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

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Scientific Coding Research Specialist

Job Description

Job Responsibility

Requirements

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Scientific Coding Research Specialist

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