36 Contract Review jobs in India

Position: Fraud Review – Analyst

About:

bluCognition is an AI/ML based start-up specializing in risk analytics, data conversion and data enrichment capabilities. Founded in 2017, by some very named senior professionals from the financial services industry, the company is headquartered in the US, with the delivery centre based in Pune. We build all our solutions while leveraging the latest technology stack in AI, ML and NLP combined with decades of experience in risk management at some of the largest financial services firms in the world.

Our clients are some of the biggest and the most progressive names in the financial services industry. We are entering a significant growth phase and are looking for individuals with entrepreneurial mindset who want to join us in this exciting journey.

Job Description:

• Monitor and identify high risk transactions within the business portfolio.

• Observe customer transactions to identify fraudulent activity such as account take over, friendly fraud, theft and similar other risks.

• Identify fraudulent transactions and cancel them from further processing.

• Resolve queued transactions within the service level agreements to reduce potential revenue losses.

• Interact with customers to validate information and to confirm or cancel authorizations.

• Monitor constantly customer and transactional records to identify unauthorized transactions and fraudulent accounts.

• Ensure confidentiality of all information collected during investigation.

• Determine existing fraud trends by analyzing accounts and transaction patterns.

• Identify system improvements to prevent fraudulent activities.

• Recommend anti-fraud processes for changing transaction patterns and trends.

• Maintain fraud analysis models, trackers to improve efficiency and effectiveness of company systems.

• Maintain the performance as per KRA.

• Undertake other responsibilities as may be assigned/approved by management from time to time.

Skills & Experience Required:

• 1+ year(s) experience in fraud investigation or KYC/AML process is preferable.

• Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy.

• Proficient in MS Office.

• Bachelor’s Degree in related field like accounting, economics, business management, statistics, etc.

• Good communication skills, with proficiency in English and to be able to communicate with the US based client directly.

Location: C - 3010, Solitaire Business Hub, Viman Nagar, Pune - , Maharashtra, India

Mode of Work: Onsite / Work from Office (WFO)

Working Days: 5 Days a Week - Mondays to Fridays Shift Timings: Day

Shift - 11 AM to 8 PM IST with slight flexibility which could be required at times

Position Overview

Quality Review Specialist will be responsible for performing a variety of loan quality check prior to closing. Candidates must possess a strong sense of urgency with an ability to work in a team environment, maintaining excellent organizational, high attention to detail, communication, and PC skills.

Essential Job Functions:

• Maintain daily workflow prioritization to ensure pipeline management meets required closing dates
• Order all required verifications, documentation and subsequent follow-ups and ensures all timeframes and compliance requirements are being met
• Should have knowledge on Paystub, W2s, Bonus-Commission, passive (Alimony-Child Support), Rental Income.
• Communicate with all parties involved in the transaction to keep them informed of file status
• Escalates fraud files to Credit Manager/Risk Management team.
• Communicate status and decisions (approval, suspense, denial) to the appropriate individuals in accordance with company SLA’s
• Strong communication skills & computer proficiency – i.e. – Microsoft Word, Excel, Electronic Mail, Internet
• Ability to perform duties under minimal supervision and actively engage with supervisor to resolve complicated issues
• Strong time management skills to plan and organize a high daily loan volume
• Provide excellent customer service to internal and external clients by demonstrating expertise, thoroughness, thoughtfulness, politeness, and enthusiasm

Requirements:

• Minimum 1 year experience in US Residential Mortgage preferably in Pre/ Post close audit with excellent knowledge of guidelines
• Excellent customer service and written and verbal communication skills
• Detail oriented and excellent organizational skills
• Quick learner to keep up with the fast paced mortgage industry
• Able to prioritize multiple tasks and manage time
• Problem-solver with strong analytical skills
• Adheres to directives, procedures, and standards
• Ability to work in a paperless environment
• Computer proficiency including Microsoft Office Product Suite
• Candidates must be available to work outside of normal business hours when necessary
• Flexible to work in 24/7 process including night shifts and weekends
• Candidate should be ok to work from office

If you have the relevant experience and interested for this role. please email me the updated profile to

Quality Review Specialist/Pre and Post Close Audit

Essential Job Functions:

• Maintain daily workflow prioritization to ensure pipeline management meets required closing dates
• Order all required verifications, documentation and subsequent follow-ups and ensures all timeframes and compliance requirements are being met
• Should have knowledge on Paystub, W2s, Bonus-Commission, passive (Alimony-Child Support), Rental Income.
• Communicate with all parties involved in the transaction to keep them informed of file status
• Escalates fraud files to Credit Manager/Risk Management team.
• Communicate status and decisions (approval, suspense, denial) to the appropriate individuals in accordance with company SLA’s
• Strong communication skills & computer proficiency – i.e. – Microsoft Word, Excel, Electronic Mail, Internet
• Ability to perform duties under minimal supervision and actively engage with supervisor to resolve complicated issues
• Strong time management skills to plan and organize a high daily loan volume
• Provide excellent customer service to internal and external clients by demonstrating expertise, thoroughness, thoughtfulness, politeness, and enthusiasm

Requirements:

• Minimum 1 year experience in US Residential Mortgage preferably in Pre/ Post close audit with excellent knowledge of guidelines
• Excellent customer service and written and verbal communication skills
• Detail oriented and excellent organizational skills
• Quick learner to keep up with the fast paced mortgage industry
• Able to prioritize multiple tasks and manage time
• Problem-solver with strong analytical skills
• Adheres to directives, procedures, and standards
• Ability to work in a paperless environment
• Computer proficiency including Microsoft Office Product Suite
• Candidates must be available to work outside of normal business hours when necessary
• Flexible to work in 24/7 process including night shifts and weekends

Greetings from Netsach - A Cyber Security Company.

We have an immediate requirement for Secure Code Review Consultant with 6 - 12 yrs experience in Banking/BFSI domain.

Job Title: Secure Code Review Consultant

Exp: 6-12yrs

Job Location: Bangalore 

Work Type: Fulltime

Interested candidates please share your profile at and kindly register in netsachglobal.com and do share your resume.

Job Description: 

TECHNICAL SPECIFICATION

Proven Technical experience reviewing of source code

Provide independent code review of bank software solutions:

- Provide review of code for new changes/solutions

- Provide review of code for existing solutions.

The code review will cover changes done in Java and C#. (Optional: Temenos T24 core banking system)

Code review may include any solutions (out-of-the-box or built) to improve turn-around time.

The code quality review will include but not limited to:

 i.   Functionality:

Check that code aligns to requirements. Are all features implemented are working as specified. Any potential negative cases and error conditions handled appropriately including all error handling. 

ii.   Code Quality:

Ensure code is optimized for efficiency, performance and resource usage. Resources to recommend fixes and best practice to attaining functionality.

iii.   Security and vulnerability checks:

Ensure security/Vulnerability have been taken care of including validation of user inputs, data protection.

iv.   Other Considerations:

Ensure reusability of code and all dependencies are declared correctly.

F) Provide report to management on:

 Thematic Issues identified and recommended solutions

 Threats and vulnerabilities

• Recurring issues

Thank You

Emily Jha

Netsach - A Cyber Security Company

Job Title / Primary Skill: Associate Medical Data Review Manager

Years of Experience: 2 + Years.

Job Location: Bangalore/Thane (Hybrid)

Educational qualification: MBBS/MD is a must.

Job Overview:

• Serve as a Subject level Data reviewer (SLDR) and identify any anomalies in patient reported data by performing Subject
• Level Data Review that requires further investigation with the clinical site to determine overall accuracy
• Conduct in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data)
• Provide project management to the team in the area of Project Management and viewed as an expert in data management.
• Drive the delivery of end-to-end study data quality and integrity.
• Provide medical, clinical, and scientific advisory expertise.
• May act as a clinical data scientist for performing data analytics by reviewing the visualizations, identify potential issues of concern and present at multi-disciplinary team meetings and external meetings.
• Ensure data quality focus to audit readiness with Clinical Compliance and Systems Validation Compliance. .
• Define data capture requirements in line with protocol and reporting needs.
• Maintain strong customer relationships
• Ensure timely follow-up and resolution of compliance issues
• Serve as Subject Matter Expert (SME)
• Serve as POC/ Back-up POC

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Good understanding of clinical/medical data.
• Knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology.
• Proven expertise in the proactive identification of issues.
• Demonstrated ability to plan, organize and manage resources to bring to successful completion specific study or project goals and objectives in accordance with defined quality and time based metrics.
• Proven ability to work within a matrix team environment requiring minimum level of supervision

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

• MBBS or MD with 2 + years of work experience.
• Experience in clinical data sciences at a CRO, pharmaceutical company or other medical environment with demonstrated leadership experience

**Working with Us**
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
**Key Responsibilities**
As an Individual contributor:
The Annual Product Review (APQR) Manager-Will primarily manage the Global BMS site APQR program by authoring and completing the APQRs for all BMS commercial Marketed Products. The APQR manager will be responsible for the completion of this annual compliance expectation by partnering with the site to draft and compete document from final approval.
The APQR specialist will be responsible for the following defined roles and responsibilities:
+ Responsible to provide oversight and completion of the site APQRs
+ Responsible for authoring through approval of APQRS assigned, per site APQRs per schedule
+ Responsible for ensuring any site or CMO APQR is created following the effective process and procedures
+ Responsible for updates to the APQR program requiring SOP, WI and/or training
+ Provide in depth quality and compliance oversight during report authoring and reviewing.
+ Responsible for ensuring all elements of the AQPR procedure are compliantly fulfilled.
+ Responsible for facilitating review and approval meetings, problem-solving key issues, and effectively managing communications with key stakeholders.
+ Responsible to escalate any deficiencies in the draft APQR which cannot be resolved with the working team
+ Responsible for projecting and communicating stakeholder actions and timing.
+ Responsible for escalation of risk to management if not meeting the completion date.
+ Responsible for providing opportunities for process improvement and standardization.
+ Supporting onboarding and training of more junior team members
+ Support, as required, the implementation and/or maintenance of additional QA Systems, which may include (but is not limited to) APQR program documentation, Change Control, Quality Risk Management, Product Quality Complaints and Annual Product Quality Reviews
+ Support, as required, Digitalization/automation/efforts for the APQR program
**Qualifications & Experience**
**Specific Knowledge, Skills, Abilities:**
+ Demonstrated knowledge of Biologics, Pharmaceutical, and/or Cell Therapy operations and processes required.
+ Completes work with periodic check in with direct manager
+ Experience in a GMP Quality role required in a commercial operations setting
+ Demonstrated experience in authoring and completing site APQRs
+ Ability to drive consensus, performance and to lead strategically
+ Prior experience with navigating multiple Quality Management systems.
+ Demonstrated strategic and tactical thinking capability with strong project management skills and ability to focus on execution of strategic decisions.
+ Solid negotiating and influencing skills in a matrixed organization.
+ Ability to work in a global matrix environment.
+ Ability to build strong relationships by being transparent, reliable, and delivering on commitments.
+ Effective communication skills.
+ Ability to provide innovative ideas, align and make decisions balancing speed, quality, and risk.
+ Fluent in English, with proven professional working proficiency in English for reading, writing and speaking.
**Education:**
+ Minimum 5 years of experience in a quality, and/or regulatory role within the biopharmaceutical industry with demonstrated expertise in Quality Compliance, or Operations preferred.
**Travel:**
+ Must have ability to travel to US required (specifically for training purposes)
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
**Uniquely Interesting Work, Life-changing Careers**
With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
**On-site Protocol**
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit careers.bms.com/ ( eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
**Company:** Bristol-Myers Squibb
**Req Number:** R
**Updated:** :01:00.082 UTC
**Location:** Hyderabad-IN
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

**Global HEOR Systematic Literature Review Manager**
**Department: Global Health Economics & Outcomes Research (HEOR)**
**Job Family: Health Economics**
**Job Type: Full-Time**
**Location: Hyderabad, India**
**Reports To: Global Systematic Literature Review Team Lead**
**Position Summary**
The Global Systematic Literature Review (SLR) Manager provides expertise in designing, executing, and managing literature review services within Amgen's Global HEOR function. The SLR Manager will collaborate closely with Global HEOR Product Leads to align with HEOR product strategy. This role supports global access to Amgen's therapies through the generation of high-quality, evidence-based outputs across the product lifecycle.
**Key Responsibilities**
+ Refine literature review questions in alignment with Global HEOR Product Lead and prepare research protocols.
+ Develop inclusion/exclusion criteria within the PICO framework.
+ Design literature searches for electronic databases (e.g., PubMed, EMBASE, Cochrane Library) and grey literature (e.g., conference proceedings, regulatory sites).
+ Screen abstracts and full-texts to determine relevance based on PICO criteria.
+ Create and review PRISMA diagrams to document full-text study selection.
+ Develop and validate data abstraction tools; finalize analyzable datasets.
+ Draft evidence tables, figures, final reports, and presentation decks, interpreting patterns and trends.
+ Manage project timelines and deliverables.
+ Conduct training and onboarding for literature review tools and platforms.
+ Experience of working with literature review platforms and AI tools
+ Knowledge and experience of conducting meta-analyses
+ People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEOR teams across various time zones
**Qualifications**
**Education**
+ Bachelor's or Master's degree in pharmacy, health economics, public health, medicine, epidemiology, or a related health sciences field.
**Experience**
+ Years of relevant experience in systematic literature review methods in the pharmaceutical, biotech or consulting setting: + **6 years for Master's degree and +8 years for Bachelor's degree.**
+ Experience in evidence synthesis feasibility assessments and network meta-analysis is preferred.
+ Proficiency in biomedical databases (e.g., MEDLINE, Embase).
+ Strong understanding of research principles and implementation.
**Skills & Competencies**
+ Excellent English oral and written communication, with ability to tailor content to different stakeholders; past medical writing experience is a plus
+ Skilled with EndNote or other reference management tools (preferred).
+ Proficiency with Microsoft Office (Word, PowerPoint, Excel).
+ Experience on systematic review tools and citation databases (e.g., PubMed, EMBASE);
+ High attention to detail and strong editing/fact-checking abilities.
+ Innovative use of artificial intelligence to boost efficiency
**Organizational Behaviors**
+ Team-oriented with demonstrated collaboration.
+ Capable of managing multiple projects simultaneously.
+ Comfortable working in a global team across time zones and cultures.

**Working with Us**
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
**Key Responsibilities**
As an Individual contributor:
The Annual Product Review (APQR) Specialist -Will primarily manage the Global BMS site APQR program by leading and generating the APQRs for all commercial Marketed Products. The APQR specialist will be responsible for the completion of this annual compliance expectation by leading a team of Subject Matter Experts to draft and compete document from draft to final approval and delivery to the key stakeholders in alignment with the prescribed schedule.
The APQR specialist will be responsible for the following defined roles and responsibilities:
+ Responsible to provide oversight and completion of the site APQRs
+ Responsible for authoring of APQRS assigned, per site APQRs per schedule
+ Responsible for ensuring any site or CMO APQR is created following the effective process and procedures
+ Provide in depth quality and compliance oversight during report authoring.
+ Responsible for ensuring all elements of the AQPR procedure are fulfilled accurately.
+ Responsible for facilitating review and approval meetings, problem-solving key issues, and effectively managing communications with key stakeholders.
+ Responsible for collecting review feedback and resolving comments and questions.
+ Responsible for projecting and communicating stakeholder actions and timing.
+ Responsible to escalate any deficiencies in the draft APQR which cannot be resolved with the working team
+ Responsible for escalation of risk to not meeting the completion date.
+ Responsible for providing opportunities for process improvement.
+ Accountable to adhere to GMPs and BMS Policies and Procedures
+ Support as may be required, the implementation and/or maintenance of additional QA Systems, which may include (but is not limited to) APQR program documentation, Change Control, Quality Risk Management, Product Quality Complaints and Annual Product Quality Reviews
+ Support as required Digitalization/automation/efforts for the APQR program
**Qualifications & Experience**
**Specific Knowledge, Skills, Abilities:**
+ Understanding of Biologics, Pharmaceutical, and/or Cell Therapy operations and processes required.
+ Works with the routine oversight on direct manager.
+ Experience in a GMP Quality role required
+ Experience in authoring APQRs
+ Prior experience with navigating Quality Management systems.
+ Demonstrated tactical thinking capability with strong project management skills.
+ Ability to work in a global environment.
+ Demonstrated negotiating and influencing skills in a matrixed organization.
+ Ability to build strong relationships by being transparent, reliable, and delivering on commitments.
+ Effective communication skills.
+ Ability to provide innovative ideas, align and make decisions balancing speed, quality, and risk.
+ Fluent in English, with proven professional working proficiency in English for reading, writing and speaking.
**Education:**
+ Minimum 3 years of experience in a technical, quality, and/or regulatory role within the biopharmaceutical industry with demonstrated acumen in Quality Compliance or Operations preferred.
**Travel:**
+ Must have ability to travel to US required (specifically for training purposes)
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
**Uniquely Interesting Work, Life-changing Careers**
With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
**On-site Protocol**
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit careers.bms.com/ ( eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
**Company:** Bristol-Myers Squibb
**Req Number:** R
**Updated:** :01:00.082 UTC
**Location:** Hyderabad-IN
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

**Global HEOR Systematic Literature Review Senior Associate**
**Department: Global Health Economics & Outcomes Research (HEOR)**
**Job Family: Health Economics**
**Job Type: Full-Time**
**Location: Hyderabad, India**
**Reports To: Global Systematic Literature Review Team Lead**
**Position Summary**
The Global Systematic Literature Review (SLR) Senior Associate provides expertise in designing, executing, and managing literature review services within Amgen's Global HEOR function. The SLR Senior Associate will collaborate closely with team lead and Global HEOR Product Leads to align with HEOR product strategy. This role supports global access to Amgen's therapies through the generation of high-quality, evidence-based outputs across the product lifecycle.
**Key Responsibilities**
+ Refine literature review questions in alignment with team lead and prepare research protocols.
+ Design literature searches for electronic databases (e.g., PubMed, EMBASE, Cochrane Library) and grey literature (e.g., conference proceedings, regulatory sites).
+ Screen abstracts and full-texts to determine relevance based on PICO criteria.
+ Create and review PRISMA diagrams to document full-text study selection.
+ Extract data from included articles into a predefined data extraction template
+ Draft evidence tables, figures, final reports, and presentation decks, interpreting patterns and trends.
+ Ensure quality of assigned work
+ People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEOR teams across various time zones
**Qualifications**
**Education**
+ Bachelor's or Master's degree in pharmacy, health economics, public health, medicine, epidemiology, or a related health sciences field.
**Experience**
+ Years of relevant experience in systematic literature review methods in the pharmaceutical, biotech or consulting setting: **+3 years for Master's degree and +5 years for Bachelor's degree.**
+ Experience of conducting different types of literature reviews (clinical, economic, QoL, burden of illness etc.)
+ Able to prioritize and manage multiple projects with high efficiency in first pass, second pass and data extraction milestones
+ Proficiency in biomedical databases (e.g., MEDLINE, Embase).
+ Strong understanding of research principles and implementation.
**Skills & Competencies**
+ Excellent English oral and written communication, with ability to tailor content to different stakeholders; past medical writing experience is a plus
+ Skilled with EndNote or other reference management tools (preferred).
+ Proficiency with Microsoft Office (Word, PowerPoint, Excel).
+ Experience on systematic review tools and citation databases (e.g., PubMed, EMBASE);
+ High attention to detail and strong editing/fact-checking abilities.
+ Innovative use of artificial intelligence to boost efficiency
**Organizational Behaviors**
+ Team-oriented with demonstrated collaboration.
+ Capable of managing multiple projects simultaneously.
+ Comfortable working in a global team across time zones and cultures.