CrawlJobs Logo

Associate Director - Skills and Learning Advisory

us.gsk.com Logo

GSK

Location Icon

Location:
India , Bengaluru

Category Icon

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided

Job Description:

The role leads the Skills and Learning Advisory team and serves as a strategic partner to the Learning Centre of Excellence and advisor to LBPs across the end-to-end learning value chain. It provides business units with expert guidance on skills management and development via the Learning Experience Platform, drives demand management and optimization, and oversees learning communications. The post-holder will also lead the design and delivery of learning initiatives and programmes to meet BU priorities, and will collaborate closely with Global Talent, Leadership and Learning teams on transformation work and other global projects.

Job Responsibility:

  • Execute the learning strategy by developing learning plans and curricula for CoE and BU initiatives, partnering with stakeholders across the enterprise to assess and prioritize learning needs.
  • Lead & manage an experienced team of skill & learning advisors to navigate & deliver the business and Talent, Learning & Capability Development learning priorities.
  • Own Learning Traffic Control and demand management for assigned BUs—prioritize requests, allocate resources, and ensure timely delivery aligned to BU priorities.
  • Lead demand planning and forecasting with BUs to anticipate capacity and business-specific initiative requirements.
  • Schedule programmes and learning initiatives according to demand and resource availability, ensuring on-time multi-country deployment.
  • Translate concepts into delivery by leading design, commissioning (in-house vs external) and execution of learning initiatives that meet BU learning agendas.
  • Lead communications, marketing and learner engagement for global, regional and local projects, and provide ongoing customer learning support.
  • Create and maintain dashboards and reports tracking programme performance, demand, adoption and impact, and provide actionable insights to stakeholders.
  • Develop and manage on-demand resources and self-facilitated sessions
  • coordinate logistics and delivery across geographies and sites.
  • Triage incoming requests to optimise allocation between internal design work and external vendor commissioning.
  • Identify and drive content optimisation and re-use opportunities where duplicate or fit-for-purpose materials exist.
  • Ensure consistent integration of the GSK Learning brand across content and learning communications.
  • Support the CoE and LBPs in creating and maintaining learning pathways and in rolling out the L&D Hub to drive adoption and engagement across all BUs.
  • Support BUs to scale delivery and measure learning impact and value against business objectives.
  • Manage relationships with external partners and vendors supporting business-specific learning initiatives.
  • Drive service performance and adherence to standard approaches and agreed timelines
  • coach and mentor the team while modelling GSK values and behaviours.
  • Collaborate closely with Global Talent, Leadership and Learning teams on transformation initiatives and other global projects, and partner with wider L&D operations to share best practices and capacity.

Requirements:

  • Bachelors or Masters’s degree with total 16+ years of experience
  • Experience of managing large enterprise wide Global learning programmes and large teams
  • Knowledge of LXP, LMS and ticketing systems
  • Experience of leading activities for a change in Ways of Working
  • Knowledge and Experience of Learning Processes and systems Project Management Experience
  • Excellent interpersonal skills and the ability to build effective relationships.
  • Demonstrated experience managing others or successfully leading without authority across matrix teams
  • Experience of initiating or participating in significant Process Creation or Improvement activities and projects.
  • Proven ability to lead and influence others both within and without direct line responsibility and to manage in a matrix environment.
  • Demonstrated analytical skills and experience of working with data and metrics.
  • Experience of exercising good judgment and working with a variety of different people.
  • Demonstrated written and verbal communication skills.
  • Experience in managing larger projects is preferred
  • Experience in / knowledge of learning communications & marketing
  • Certifications in Learning Design, Performance Consulting, Program Management preferred

Nice to have:

  • Experience in managing larger projects is preferred
  • Experience in / knowledge of learning communications & marketing
  • Certifications in Learning Design, Performance Consulting, Program Management preferred
What we offer:
  • Competitive base salary
  • Annual bonus based on company performance
  • Flexible working options available for most roles
  • Learning and career development
  • Access to healthcare & wellbeing programmes
  • Employee recognition programmes

Additional Information:

Job Posted:
March 27, 2026

Employment Type:
Fulltime
Job Link Share:

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

Briefcase Icon

Similar Jobs for Associate Director - Skills and Learning Advisory

Private Client Tax Associate Director

Our client, a leading firm of Chartered Accountants in Edinburgh, is seeking a t...
Location
Location
United Kingdom , Edinburgh
Salary
Salary:
70000.00 - 100000.00 GBP / Year
https://crowewatson.co.uk/ Logo
Crowe Watson
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • CTA/ACA/ACCA qualified (or equivalent)
  • Significant experience in private client tax advisory within a senior role
  • Strong technical knowledge of UK tax legislation and planning
  • Must have a minimum of 5 years previous experience working within a UK Practice environment
  • Excellent communication and relationship management skills
  • A proactive, strategic mindset with a commercial approach to client service
Job Responsibility
Job Responsibility
  • Provide strategic tax planning and advisory services to high-net-worth individuals, trusts, and business owners
  • Lead and manage a portfolio of private clients, ensuring exceptional client service and compliance
  • Develop and mentor junior team members, fostering a culture of continuous learning and development
  • Identify new business opportunities and contribute to the firm’s growth strategy
  • Stay up to date with legislative changes and ensure clients receive proactive tax advice
What we offer
What we offer
  • flexible working
  • company pension
  • Fulltime
Read More
Arrow Right

Medical Science Liaison

As a Medical Science Liaison, you will advance medical science through clinical ...
Location
Location
Algeria , Algiers
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Excellent product knowledge and expertise
  • Outstanding presentation and communication skills in both the local language and English
  • Proven teaching capabilities and an understanding of adult learning concepts
  • Effective critical thinking skills and strategy implementation
  • A broad understanding of the regulatory and healthcare environment in the country/region
  • Excellent organizational skills, resilience, and empathy
  • An MD and/or PhD and/or equivalent healthcare qualifications, preferably with proven MSL experience
  • 2-3 years post-graduate experience within the healthcare industry
  • Clinical trial experience with knowledge of GCP
  • Training in adverse event reporting
Job Responsibility
Job Responsibility
  • Identifies and advances clinical needs, ensuring that we continually meet the evolving requirements of the healthcare community
  • Acts as the primary contact for investigator-initiated trials, facilitating the successful implementation of research initiatives
  • Assists in the development of publication plans to share new findings and insights with the broader medical community
  • Supports the medical manager in the review of promotional materials, ensuring they comply with the highest standards of accuracy and compliance
  • Acts as a liaison with the medical community, including medical professional societies, opinion leaders, investigators, and consultants
  • Supports the medical director/medical manager in collaborating with opinion leaders
  • Provides accurate and balanced medical-scientific education and information on products, therapies, issues, trends, and clinical research
  • Conducts demonstrations and in-services at customer sites
  • Assists in the development of medical-scientific advisory boards, symposia, and educational forums
  • Educates and trains internal staff on products and therapies
  • Fulltime
Read More
Arrow Right

Medical Science Liaison

As a MEDICAL SCIENCE LIAISON in Algeria at Baxter you will play a pivotal role i...
Location
Location
Algeria , Algiers
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Excellent product knowledge and expertise
  • Outstanding presentation and communications skills in both the local language and English
  • Proven teaching capabilities and an understanding of adult learning concepts
  • Effective critical thinking skills and strategy implementation
  • A broad understanding of the regulatory and healthcare environment in the country/region
  • Excellent organizational skills, resilience, and empathy
  • An MD and/or PhD and/or equivalent healthcare qualifications, preferably with proven MSL experience
  • 2-3 years post-graduate experience within the healthcare industry
  • Clinical trial experience with knowledge of GCP
  • Training in adverse event reporting
Job Responsibility
Job Responsibility
  • Identifies and advances clinical needs, ensuring that we continually meet the evolving requirements of the healthcare community
  • Acts as the primary contact for investigator-initiated trials, facilitating the successful implementation of research initiatives
  • Assists in the development of publication plans to share new findings and insights with the broader medical community
  • Supports the medical manager in the review of promotional materials, ensuring they compete with the highest standards of accuracy and compliance
  • Acts as a liaison with the medical community, including medical professional societies, leaders with a point of view, visionaries, investigators, and consultants
  • Supports the medical director/medical manager in collaborating with leaders with a point of view, encouraging relationships that drive innovation and excellence in medical science
  • Provides accurate and fair-balanced medical-scientific education and information on products, therapies, issues, trends, and clinical research
  • Conducts demonstrations and in-services at customer sites to ensure flawless clinical use of products
  • Assists in the development of medical-scientific advisory boards, symposia, and other educational forums
  • Educates and trains internal staff on products, therapies, issues, trends, and clinical research, ensuring our team remains at the forefront of medical knowledge
  • Fulltime
Read More
Arrow Right

Medical Director, Global Evidence Generation Lead

The medical Director, evidence generation is responsible for supporting strategi...
Location
Location
Belgium , Mechelen
Salary
Salary:
Not provided
it.alfasigma.com Logo
Alfasigma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 7+ years of experience in evidence generation, clinical development, HEOR, or a related field
  • At least 5 years of experience in Epidemiology, Health Economics Outcomes Research (HEOR), or/and Health Systems Research
  • Proven track record of developing and implementing integrated evidence generation plans in the pharmaceutical or biotechnology industry
  • Experience in design, conduct and oversight of real-world evidence studies ranging from protocol writing to project management oversight and data interpretation and communication
  • Solid understanding of the cross functional drug development lifecycle and processes (Business Development, clinical trial design, conduct, & endpoint selection, Clinical Operations, Data Management, Biostatistics, and Regulatory)
  • Demonstrated expertise and experience working with methods for evidence generation using primary and secondary data sources, knowledge of common issues and challenges of implementation, and track-record of successful publications
  • Demonstrated depth of understanding of observational research methods, regulatory standards, and ability to leverage epidemiologic and data science expertise to meet evolving business needs
  • Evidence of technical expertise of applying pharmacoepidemiology evidence and insights at the therapy/product level
  • Ability to explain strengths and limitations of clinical practice datasets — such as electronic health records, claims, clinical data registries, patient generated health data, and other health data sources — in context of designing pharmacoepidemiology study designs
  • Ability to work successfully in a matrix and quick paced environment
Job Responsibility
Job Responsibility
  • Collaborate with cross-functional colleagues to Lead the development and execution of Medical evidence generation strategy and tactics supporting products in development as well as those commercially available, with appropriate prioritization and use of resources ensuring alignment with corporate goals, regional needs, and therapeutic priorities
  • Oversee the Design and implementation of Integrated Evidence Generation Plans (IEGPs) that incorporate clinical, real-world, and economic data to support product positioning and value demonstration
  • Scope RWE studies (Regional/National/Academic/Patient/Vendor), selection of new or existing academic (can include: ISR/lIS/NIS)/non-governmental registries (retrospective/prospective), management across various phases from start up, maintenance to final deliverables
  • Translate (early) trial efficacy to real-world comparative effectiveness as part of early and late phase study planning, identification of subpopulations, and for potential risk-sharing purposes
  • Design and implement multiple database and/or de novo (e.g. registries) pharmacoepidemiologic studies, as well as literature reviews, intended to provide insight into background epidemiology, disease state regular care, and/or quantify benefits and/or risks potentially associated with Alfasigma products
  • Project management oversight – ensuring effective design, initiation and implementation of real world evidence studies, while ensuring effective study protocols and plans, managing budget and milestone tracking, and where appropriate contracting with partner organizations
  • keep abreast on new data and developments in the field, key publications of interest, research methodologies and regulatory standards across the EU and New Markets regions and proactively address HOR strategy changes in collaboration with global and regional teams in anticipation of any trends
  • Review and provide relevant RWE/HOR inputs to statistical analysis plans and analysis outputs
  • Understand the legal and compliance environment and drive collaboration with the Legal and Compliance team
  • Establish metrics to evaluate the effectiveness and impact of evidence generation activities on corporate and product-specific objectives
What we offer
What we offer
  • We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development
Read More
Arrow Right

Senior Manager, Evidence Generation Lead

The medical Director, evidence generation is responsible for supporting strategi...
Location
Location
Belgium , Mechelen
Salary
Salary:
Not provided
it.alfasigma.com Logo
Alfasigma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 7+ years of experience in evidence generation, clinical development, HEOR, or a related field, with at least 5 years of experience in Epidemiology, Health Economics Outcomes Research (HEOR), or/and Health Systems Research
  • Proven track record of developing and implementing integrated evidence generation plans in the pharmaceutical or biotechnology industry
  • Experience in design, conduct and oversight of real-world evidence studies ranging from protocol writing to project management oversight and data interpretation and communication
  • Solid understanding of the cross functional drug development lifecycle and processes (Business Development, clinical trial design, conduct, & endpoint selection, Clinical Operations, Data Management, Biostatistics, and Regulatory)
  • Demonstrated expertise and experience working with methods for evidence generation using primary and secondary data sources, knowledge of common issues and challenges of implementation, and track-record of successful publications
  • Demonstrated depth of understanding of observational research methods, regulatory standards, and ability to leverage epidemiologic and data science expertise to meet evolving business needs
  • Evidence of technical expertise of applying pharmacoepidemiology evidence and insights at the therapy/product level
  • Ability to explain strengths and limitations of clinical practice datasets — such as electronic health records, claims, clinical data registries, patient generated health data, and other health data sources — in context of designing pharmacoepidemiology study designs
  • Ability to work successfully in a matrix and quick paced environment
  • Ability to multitask priorities to align with program objectives
Job Responsibility
Job Responsibility
  • Collaborate with cross-functional colleagues to Lead the development and execution of Medical evidence generation strategy and tactics supporting products in development as well as those commercially available, with appropriate prioritization and use of resources ensuring alignment with corporate goals, regional needs, and therapeutic priorities
  • Oversee the Design and implementation of Integrated Evidence Generation Plans (IEGPs) that incorporate clinical, real-world, and economic data to support product positioning and value demonstration
  • Scope RWE studies (Regional/National/Academic/Patient/Vendor), selection of new or existing academic (can include: ISR/lIS/NIS)/non-governmental registries (retrospective/prospective), management across various phases from start up, maintenance to final deliverables
  • Translate (early) trial efficacy to real-world comparative effectiveness as part of early and late phase study planning, identification of subpopulations, and for potential risk-sharing purposes
  • Design and implement multiple database and/or de novo (e.g. registries) pharmacoepidemiologic studies, as well as literature reviews, intended to provide insight into background epidemiology, disease state regular care, and/or quantify benefits and/or risks potentially associated with Alfasigma products
  • Project management oversight – ensuring effective design, initiation and implementation of real world evidence studies, while ensuring effective study protocols and plans, managing budget and milestone tracking, and where appropriate contracting with partner organizations
  • keep abreast on new data and developments in the field, key publications of interest, research methodologies and regulatory standards across the EU and New Markets regions and proactively address HOR strategy changes in collaboration with global and regional teams in anticipation of any trends
  • Review and provide relevant RWE/HOR inputs to statistical analysis plans and analysis outputs
  • Understand the legal and compliance environment and drive collaboration with the Legal and Compliance team
  • Establish metrics to evaluate the effectiveness and impact of evidence generation activities on corporate and product-specific objectives
What we offer
What we offer
  • We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development
Read More
Arrow Right

Global Trade Operations Associate Director

Owens Corning is looking for a trade professional to join our team as our Global...
Location
Location
United States , Toledo
Salary
Salary:
125000.00 - 175000.00 USD / Year
owenscorning.com Logo
Owens Corning
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Undergraduate degree, advanced degree (i.e. MBA) or other significant industry experience such as U.S. Customs Broker License required
  • At least 10 years relevant experience in logistics, trade compliance or a related field
  • Experience working in a multinational company with cross-functional collaboration that relies heavily on relationship building to succeed.
  • Strong analytical skills with the ability to interpret complex trade data and identify actionable insights.
  • Deep knowledge of U.S. Canada and Mexico trade regulations, with experience navigating import/export controls and compliance frameworks.
  • Technologically proficient
  • comfortable working with trade systems, analytics platforms, and automation tools.
  • Proven ability to lead through influence and build strong cross-functional partnerships across global teams.
  • Thoughtful communicator with excellent stakeholder engagement skills, capable of inspiring collaboration and alignment.
  • Demonstrated success in developing high-performing teams and fostering a culture of innovation, curiosity, and continuous learning.
Job Responsibility
Job Responsibility
  • Own and execute the operational trade strategy for North America, including import/export controls, broker management, and service provider oversight.
  • Lead the development and implementation of effective controls for high-impact processes, ensuring alignment with internal control frameworks.
  • Coordinate global and regional trade compliance risk assessments and implement mitigation plans in collaboration with the Director of Global Trade and Trade Data & Risk Management teams.
  • Manage export licensing, jurisdictional determinations, and technology control plans.
  • Oversee the Global Sanctions program, including service provider compliance and escalation procedures.
  • Manage and escalate issues related to global sanctions, restricted party screening, and anti-boycott regulations.
  • Lead escalation protocols for significant compliance violations or government inquiries
  • Build strategic partnerships across key functions including Sourcing, Planning, Sales, Customer Service, Warehouse, Manufacturing, Engineering, Finance, Tax, Accounting, Sustainability, EH&S, and Legal.
  • Develop strong relationships with customs brokers, freight forwarders, and trade advisory partners
  • co-lead quarterly performance reviews and implement broker scorecards and KPIs.
What we offer
What we offer
  • insurance (medical/dental/vision/life/disability/supplemental offerings)
  • 401k (company contribution regardless of employee participation – plus match)
  • liberal paid time off (vacation, personal floating and standard holidays)
  • Employee Assistance Services
  • Stock Purchase Program
  • Fulltime
Read More
Arrow Right
New

Associate Medical Director, US Medical Affairs

The Associate Medical Director will be responsible for contributing to and parti...
Location
Location
United States , Morristown
Salary
Salary:
180000.00 - 210000.00 USD / Year
it.alfasigma.com Logo
Alfasigma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • MD/PhD/PharmD (or equivalent) with a minimum of 5 years of professional/clinical experience
  • At least 3 years of biopharmaceutical industry experience in Medical Affairs and/or Clinical Research is required
  • Experience working with professional societies and quality organizations preferred
  • Prior experience in Hepatology, Gastroenterology, or Immunology preferred
  • Ability to travel up to 20% required (mostly to congresses/ad boards), which may include overnight and/or weekend travel
  • Strong understanding of Medical Affairs functions, processes, and strategic execution
  • Track record of being held accountable for key individual deliverables with successful results required
  • Strong verbal and written communication skills are essential, including strong presentation skills
  • Excellent organization and multi-tasking skills
  • Strong interpersonal skills and problem-solving capabilities
Job Responsibility
Job Responsibility
  • Participate in the development of a cross-functionally aligned set of medical strategies for the US market needs, focused on commercialized as well as late-stage development indications/assets
  • Develop the strategy for professional medical association engagement in the US in conjunction with other US stakeholders as part of the broader professional society strategy
  • Support medical affairs data generation and dissemination working group(s) and collaborate with the Scientific Communications team to develop and execute aligned strategies/tactics for maximizing our scientific communication efforts
  • Support field medical activities and help to assess and address internal/external medical education needs in collaboration with the Field Medical and Scientific Communications teams
  • Perform scientific and clinical training for internal staff, including Commercial/Sales, on Alfasigma products and respective disease-related aspects
  • Lead and execute scientific advisory boards to generate strategic insights that inform medical affairs plans
  • Participate in or perform review of promotional and medical/scientific materials as the Medical Reviewer, following standard operating practices (SOPs) and in collaboration with Regulatory, Legal, and Commercial counterparts
  • Maintain strong relationships with the external thought leader and influencer communities
  • Contribute to, and support execution of the lifecycle management activities for Alfasigma’s commercialized indications/assets
  • Understand the legal and compliance environment and drive collaboration with the Legal and Compliance team
What we offer
What we offer
  • 401(k) plan with company match
  • Rewards and recognition program
  • Health care benefits (medical, prescription drugs, dental, and vision insurance)
  • Short and long-term disability coverage provided
  • Plan coverage for domestic partners
  • Paid parental leave benefits and adoption assistance
  • Tuition reimbursement assistance
  • A generous Paid Time Off program that includes 20 vacation days, 11 holidays, 4 personal days, and 2 volunteer days per calendar year
  • Numerous well-being and work/life programs
  • Fulltime
Read More
Arrow Right

Ambulatory nursing supervisor-- Heart Rhythm Management; Device

Under the supervision of the Dir of Nursing - Ambulatory and Nurse Manager - Amb...
Location
Location
United States , Kansas City
Salary
Salary:
Not provided
kansashealthsystem.com Logo
The University of Kansas Health System
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor Degree Nursing
  • 2 or more years of RN experience
  • 1 or more years of Ambulatory experience
  • Demonstrated leadership, communication and interpersonal skills
  • Licensed Registered Nurse (LRN) - Multi-State - State Board of Nursing Must have current active multistate state Register Nurse (RN) license in good standing in state in which you live OR active single state RN license in good standing in the state you will be working with proof of application of a multistate RN license in the state in which you live
  • Basic Cardiac Life Support (BLS or BCLS) - American Heart Association (AHA) upon Hire
  • Advanced Cardiac Life Support (ACLS) - American Heart Association (AHA) upon Hire
Job Responsibility
Job Responsibility
  • Maintains current knowledge of and ensures compliance with all regulatory and professional standards of care
  • Assists the Ambulatory Clinic Manager in daily clinical and operational aspects of the clinic including staff scheduling and monitoring of provider clinic schedules to ensure effective resource management and quality improvement through monitoring of clinic key performance indicators
  • Assists with urgent EP referrals and work in appointments
  • Collaborates with the Ambulatory Clinic Manager, Senior Administrator/Director, and Physician leadership to establish patient care standards and evaluates staff compliance
  • Serves as a mentor for excellence in clinical practice and patient and employee satisfaction
  • Maintains a safe and caring environment for patients that is conducive to positive health teaching and maintenance, meeting patient and family expectations for care while implementing mechanisms to ensure culturally specific care
  • Responds to patient and family concerns or complaints with sensitivity and compassion in a timely fashion
  • Uses findings from patient and staff satisfaction surveys, complaints, and patient safety events/root cause analysis to plan and improve patient care using active mentoring and performance management strategies including MDI (monitoring daily improvement) boards
  • Assists with hiring, education and performance evaluation of the staff
  • Guide staff through prolonged orientation (6 months - 1 year) with frequent check-ins and knowledge assessments
  • Fulltime
Read More
Arrow Right