Unsolicited applications Job at NTT DATA (Valby)

Unsolicited Applications - The British School - Administration & Support Services

At The British School in Madrid, part of the Inspired Education Group, we are al...

Location

Spain , Madrid

Salary:

Not provided

International School of Bergamo

Expiration Date

Until further notice

Requirements

Previous experience in similar roles, preferably in educational or customer service settings
Strong organisational, communication, and teamwork skills
A proactive, detail-oriented, and solution-focused approach
Basic digital literacy and comfort with relevant tools (depending on the role)
A good level of English is a strong advantage
A commitment to the school’s educational mission and values

Job Responsibility

Ensuring the smooth running of the school’s administrative, operational, or technical services
Providing a professional, approachable, and solution-oriented service to families, students, and teaching staff
Managing documentation, databases, and resources according to your area of work
Collaborating with other departments to ensure a seamless educational experience
Taking part in the continuous improvement of internal processes
Adhering to school policies and regulations, especially in relation to health & safety, safeguarding, and inclusion

Sr. MSL, Medical

Location

China , Nanjing

Salary:

Not provided

BioLife Plasma Services

Expiration Date

Until further notice

Requirements

Master degree in Medical or Life science is required
doctoral education is preferred
Either ≥1 year working experience in clinical practice and/or in multinational pharmaceutical company or ≥2 year relevant work experience
For senior MSL, ≥2 prior MSL experience with a track record of success in multinational pharmaceutical company are required
Clinical experiences within relevant TAs are preferred
Fundamental knowledge of clinical study methodology
Customer focused with excellent communication and influencing skills that can impact at regional level
Highly medical project management skills to deliver on complex tasks within timeframe and manage milestones
Innovative sense and willing to drive a complex and changing environment and effectively manage and resolve issues of responsible products from medical perspective
Enthusiastic and self-motivated

Job Responsibility

Responsible for identifying and updating regional KOLs list to engage within assigned Therapy Area
Responsible for profiling regional KOLs, design and implement individual KOL engagement plan
Maintain robust and long-terms professional relationships with regional experts, particularly KOLs, by regular on field visit and other medical initiatives defined by KOLs engagement plan
Obtain feedback and advice about Takeda products or interesting TAs from KOLs through 1 on 1 interactions, advisory boards or medical meetings
Summarize and communicate relevant KOLs feedback to relevant internal stakeholders to support and help inform the medical strategy in line with brand plan
Train and develop speakers on the company's products
Identify potential investigators for Medical affairs study
Responsible for establishing regional medical plan and design medical initiatives, consistent with central medical strategy and regional medical needs
Responsible for developing and maintaining annual regional medical budget requests and ensuring the approval budgets are being managed and tracked
Plan, organize and conduct regional AB boards meetings in relevant TA

Fulltime

Case Manager Absenteeism

In our dynamic international organization, employee health and well-being are a ...

Location

Netherlands , Veldhoven

Salary:

Not provided

ASML

Expiration Date

Until further notice

Requirements

HBO working and thinking level
Completed ROV practical training
At least 3 years of relevant work experience in absenteeism case management
Current knowledge of social security, such as WVP, Sickness Benefits Act, WIA, Working Conditions Act, etc.
Strong affinity with vitality and sustainable employability
Due to the international nature of ASML, spoken and written English language skills are highly desirable

Job Responsibility

Manage and monitor absenteeism cases in compliance with applicable legislation (e.g. WVP, Ziektewet, WIA, Arbowet)
Act as a trusted advisor to managers, providing both solicited and unsolicited guidance on absenteeism, prevention, and reintegration
Drive effective collaboration between all stakeholders (employees, managers, occupational health providers, and external parties)
Ensure accurate and complete case administration and documentation
Identify opportunities to improve processes and actively contribute to the continuous development of Health Advisory services
Support a consistent, high-quality approach to absenteeism management across the organization

Fulltime

Medical Manager - Rare Diseases

Location

India , Mumbai

Salary:

Not provided

Sanofi

Expiration Date

Until further notice

Requirements

Doctoral degree in a scientific discipline (M.D Pharmacology/ MBBS)
Experience in pharmaceutical industry, regulatory environment, clinical or preclinical research, and knowledge of a therapeutic area disease state and treatment
Experience with basic research, drug discovery, drug development and SEE/KEE interactions
Experience/knowledge of Rare Diseases/ hematology/Hemophilia strongly preferred
Knowledge of digital health technologies and their application in clinical settings
Understanding of laboratory operations and diagnostic processes
Strategic thinking and flawless execution with proven ability to prioritize deliverables and balance risk
Strong analytical skills and affinity for problem solving
Fluency in MS Office including Excel, word and powerpoint
Exhibits integrity/trust

Job Responsibility

Participate to and execute the Medical and scientific (non-promotional) strategy for the SE Asia & India MCO portfolio/ therapeutic area of Rare Disease
Contribute to the strategic development and execution of the enhanced RD initiatives
Support the strategic deployment of the digital diagnostic platforms across COEs
Monitor and support Laboratory optimization initiatives for patient flow through diagnostic pathways
Lead the global humanitarian program in India
Support and guide high-risk screening initiatives across India
Be the trusted scientific partner to key external experts
Execute on stakeholder engagement plans to gather data, develop and share medical insights
Keep abreast of medical and scientific developments in the therapeutic field
Maintain effective and appropriate communication among internal stakeholders

Fulltime

Medical Scientific Liaison (MSL)

In this role as Medical Scientific Liaison (MSL) you will be the gastroenteritis...

Location

Saudi Arabia , Riyadh

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

Requirements

Advanced degree in life sciences (Bachelor of Pharmacy, MD, PhD, or equivalent), with licensure by the Saudi Commission for Health Specialties (SCFHS) as a practicing physician or pharmacist
Saudi National, as per SFDA regulation
Minimum 3 years of field MSL experience in the country, with established credible relationships within the local scientific and medical community
Demonstrated ability to exchange scientific ideas effectively with KOLs and colleagues, and to present clinical and medical data confidently to both small and large audiences
In-depth therapeutic competency in Inflammation, with experience in gastroenterology considered a strong plus
Ability to collaborate cross-functionally with Commercial, Marketing, Regulatory, Global Medical Affairs, and other internal functions
Good written and verbal communication skills in English

Job Responsibility

Systematically identify the scientific exchange needs of Key Opinion Leaders (KOLs), investigators, and other stakeholders in patient care
build strong peer-to-peer professional relationships
provide credible scientific expertise
and serve as a liaison between Global Medical Affairs and external partners
Develop and maintain peer-to-peer scientific relationships with thought leaders across healthcare, academia, payer, and government organisations in line with strategic territory plans, managing scientific partnerships, exchange, and compliant communication of the emerging product portfolio to meet the educational and professional needs of key customers
Present clinical and disease state information to diverse internal and external audiences — including KOLs, formulary/decision-makers, and other HCPs — and deliver therapeutic area training to Sales, Medical, and other colleagues upon request
Respond within defined timelines and quality standards to unsolicited medical information inquiries from HCPs, whether direct or escalated through the field force or other stakeholders
report adverse events per Alfasigma policy
Provide scientific liaison support to investigators involved in company-sponsored interventional or observational studies and investigator-sponsored research (ISR), identifying data gaps and escalating ISR needs within Medical Affairs
Ensure all activities comply with applicable pharmaceutical laws, regulations, and guidelines — including relevant SFDA guidelines, the Code of Ethical Practices, and company policies

What we offer

Competitive salary
Comprehensive benefits
Extensive opportunities for professional growth and development

Fulltime

Msl - North Central

The Medical Science Liaison (MSL) serves as a scientific and clinical expert wit...

Location

United States , San Mateo

Salary:

169000.00 - 215000.00 USD / Year

Dompé

Expiration Date

Until further notice

Requirements

Advanced scientific degree (PharmD, PhD, MD, OD, or equivalent) required
Minimum 2–3 years of experience in Medical Affairs or related clinical/scientific role
ophthalmology experience preferred
Strong understanding of clinical research, disease state management, and evidence-based medicine
Excellent communication and presentation skills with the ability to translate complex science into clear, balanced discussions
Demonstrated ability to work independently and manage multiple priorities in a fast-paced environment
Self-motivated, proactive, and able to build strong relationships with internal and external stakeholders
High level of integrity and commitment to compliance with PhRMA Code and company policies
Ability to travel up to 60%, including internationally (including evenings and weekends for congresses and meetings)
Clean and valid driver’s license

Job Responsibility

Engaging external experts through fair-balanced, evidence-based scientific exchange
Ensuring compliance with PhRMA Code, internal policies, and all applicable regulations
Supporting the generation and communication of scientific insights that inform Medical Affairs strategy
Contributing to pre-launch readiness and pipeline support by building disease state expertise, facilitating clinical trial awareness, and preparing for future product introductions
Conducting fair-balanced, evidence-based scientific exchange with ophthalmologists, optometrists and health care professionals
Identifying, profiling, and engaging appropriate external experts based on clinical expertise and scientific relevance
Delivering and discussing approved scientific materials, clinical data, and disease state information in accordance with PhRMA Code and internal policies
Appropriately handling unsolicited off-label questions through approved medical information processes
Accurately and timely entries of interactions and data into compliantly managed CRM systems
Systematically collecting, synthesizing, and reporting ophthalmic clinical and scientific insights from external experts

What we offer

Comprehensive medical benefits: we value access to healthcare for our patients as well as our employees
Generous vacation / holiday time off: we care about our employees and encourage a balanced lifestyle
Competitive 401(K) matching
Very generous monthly car allowance

Fulltime

Medical Science Liaison

Location

Italy

Salary:

Not provided

The Muse

Expiration Date

Until further notice

Requirements

Minimum of 3 years of professional experience following the final stage of training, including at least 2 years in clinical practice, research, or healthcare education, preferably within the pharmaceutical or biotech industry
Strong background in infectious diseases, epidemiology, vaccines, or public health
Fluency in Italian and English, with excellent written and verbal communication skills
Strong interpersonal skills with the ability to build and maintain effective professional relationships
Demonstrated ability to manage multiple projects in a field-based environment with strong prioritization and decision-making skills
Proficiency in digital tools and platforms, including MS Office (Word, Excel, PowerPoint) and virtual engagement technologies
Ability to adapt to new technologies and effectively document medical interactions
Willingness to travel extensively across Italy and occasionally internationally (approximately 50-60%)

Job Responsibility

Communicate relevant, accurate, and updated approved medical information to healthcare professionals at local, regional, and national levels, including key opinion leaders, decision-makers, professional associations, payer groups, and public health stakeholders
Provide balanced, scientifically sound responses to unsolicited medical inquiries in full compliance with applicable regulations, policies, and guidelines
Deliver scientific presentations aligned with European and Global Medical Affairs strategies
Build and maintain trusted relationships with external stakeholders and act as a scientific partner to the medical community
Facilitate communication between healthcare professionals, healthcare organizations, and Medical Affairs
Support company-sponsored clinical trials, collaborative research, and investigator-initiated studies in accordance with internal procedures
Contribute to awareness and education initiatives in close collaboration with cross-functional teams
Gather and share customer insights to support the development and refinement of medical strategies
Provide internal scientific expertise, including support for training, medical content development, and review processes
Collaborate closely with Market Access, Sales, Regulatory Affairs, Communications, Customer Services, and Medical Affairs teams locally and across EMEA

What we offer

Health Insurance
Dental Insurance
Vision Insurance
Life Insurance
Short-Term Disability
Long-Term Disability
FSA
HSA
Mental Health Benefits
Adoption Leave

Fulltime

Applications Development Tech Lead Analyst

The Business Analytics Lead Analyst will support the North America Fraud Prevent...

Location

United States , New Castle; Irving

Salary:

125760.00 - 188640.00 USD / Year

Citi

Expiration Date

Until further notice

Requirements

10+ years of hands-on experience developing in SAS, required
Knowledge of advanced SQL and/or SAS coding techniques, required
10+ years working with extremely large data sources from multiple platforms such as SQL Server, Oracle, Teradata, and Hadoop required
5+ years of hands-on experience with Hive/Hue, Python, or other Big Data tools, preferred
5+ years of hands-on knowledge of distributed platforms like Linux or Unix, preferred
Knowledge of Hadoop and mainframe platforms, preferred
5+ years of hands-on experience with SQL Server Management Studio (SSMS), preferred
Hands on data visualization experience in Tableau or Power BI, preferred
Experience in reporting and ad hoc data support, preferred
Intermediate to advanced knowledge of Microsoft Office Products (Word, Excel, PowerPoint, Access) required

Job Responsibility

Engage as technology and data SME during interactions with key internal Citi partners and external vendors to develop solutions
Develop code to extract data from various technology platforms to support Retail Bank portfolios
Develop reporting dashboards to highlight impact of fraud trends on business performance and to identify opportunities for improvement
Utilize in-depth Retail Bank business knowledge to provide proactive support to our partners (unsolicited reporting and tools)
Support key partners through data warehousing of business analytic views, data transmissions, data integrations, and process automation
Provide support for proofs of concept with new vendor tools that combat fraud applications and account takeover
Develop standards that ensure quality of execution and accuracy of business reporting
Manage ad-hoc requests for data analysis on data sources where documentation is minimal to non-existent
Utilize leadership skills
Utilize stakeholder and people management experience

What we offer

medical insurance
dental insurance
vision coverage
401k
life insurance
accident insurance
disability insurance
wellness programs
paid time off packages
planned time off (vacation)

Fulltime

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Unsolicited applications

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