CrawlJobs Logo

Director, People & Process Management, Global Study Operations

biomarin.com Logo

BioMarin Pharmaceutical

Location Icon

Location:
United States , San Rafael

Category Icon
Category:
Research and Development

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

210400.00 - 315600.00 USD / Year
Save Job
Save Icon
Apply Position

Job Description:

The Associate Director (AD)/ Director (D), Global Study Operations, will fulfill the role of People & Process Manager of Study Managers, and is accountable for the consistent application of line management and process execution across the book of work for trial delivery at BioMarin. The book of work includes the Phase -1 through Post Approval space with the Program Leads being accountable for the successful operational delivery of all the assigned studies within their program(s). In this role the AD/D is the mentor, coach, and line-manager to Study Managers and Senior Study Managers. The AD/D will drive a positive team-based culture that is conducive to attracting, retaining, and motivating the Global Study Operations team. In addition, the incumbent will be expected to contribute to the process development based on lessons learned, and innovative approaches to continuously improve the execution of trial delivery. This role combines the complexity of study execution in the early and late-stage development space, with the need for rapid development to support registration and the focus on life cycle management in the post approval space. This role will report to the Head of People and Process Management.

Job Responsibility:

  • Partner with Phase Leads and Program Directors to align on program delivery expectations for direct reports, contribute to the development of process improvements and establish best practices to enhance the execution of trial delivery across the organization.
  • Effectively lead, develop, manage, and retain high performing teams
  • set vision and purpose through goals, clear and authentic communication.
  • Ensure visibility and alignment of corporate and functional goals with individual goals.
  • Build and manage effective working relationships with other line managers and leaders to ensure effective relations to support an engagement strategy that values diversity, inclusion, and equity.
  • Build and establish a positive team through management best practices including giving timely feedback, understanding retention issues, and ensuring clear priorities.
  • Build and establish a positive work environment by encouraging mutual respect, and accountability on a functional and project level, both locally and globally to implement and deliver the study.
  • Develop and manage partnerships with key enterprise business partners, SMEs, and stakeholders to support a strong network fostering an open and collaborative environment across the global network.
  • Collaborate with key business partners and contribute to the efforts and overall success of the wider Global Study Operations team.
  • Collaborate with stakeholders and cross-functional leads aligning on the management of project scope, plan resources, maintain schedules, and facilitate open bi-directional communication.
  • Contribute to the implementation of strategies and plans to improve complex drug development processes and capabilities.
  • Ensure compliance with all SOPs, ICH-GCP guidelines, regulatory authority regulations and patient safety standards in the conduct of global clinical trial execution.
  • Establish and maintain high quality clear work standards for projects while ensuring timely delivery of customer's business requirements within the specific business initiative and project timelines.

Requirements:

  • Minimum of 10 years in the pharmaceutical industry with a BA/BS degree with a focus on life sciences, nursing, or related technical or scientific discipline or 8 years in the pharmaceutical industry with a master’s degree
  • Minimum of 3 years management experience
  • Strong leadership attributes with excellence in line management, leading, coaching, and motivating a diverse team of individuals to reach their highest potential and successfully deliver on trial and program expectations.
  • Expertise in clinical trial management and vendor oversight
  • Solid business acumen with comfort in agile delivery in a complex learning environment, including the ability to produce and present clear, concise, professionally written communications and presentations to senior level executives and stakeholders.
  • Experience in working with Learning, Development, Engagement and Talent Strategy frameworks that welcome diversity, equity, and inclusion.
  • Effective written/verbal communication and people skills, with experience influencing and fostering collaborative relations with cross-functional stakeholders at all levels.
  • Innovative mindset with proven history of championing and supporting change to positively impact the business and its stakeholders.
  • Proactive, flexible, adaptive, and successful navigation of self and team through conflict or ambiguity to seek clarity, structure, and solutions.
  • Professional maturity to engage effectively and confidentially (as warranted) with employees, vendors, and team members.
What we offer:
  • company-sponsored medical, dental, vision, and life insurance plans
  • discretionary annual bonus
  • discretionary stock-based long-term incentives
  • paid time off

Additional Information:

Job Posted:
January 22, 2026

Employment Type:
Fulltime
Work Type:
Hybrid work
Icon
BioMarin Pharmaceutical - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon

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

Briefcase Icon

Similar Jobs for Director, People & Process Management, Global Study Operations

Local Study Associate Director

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
United States
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor degree in related discipline, preferably in life science, or equivalent qualification
  • Five years of US focused clinical trial management experience, including budget oversight
  • Good knowledge of international guidelines ICH- GCP as well as relevant local regulations
  • Excellent project management skill
  • Excellent team building and interpersonal skills
  • Excellent organisational skills
  • Excellent verbal and written communication skills
  • Excellent ability to prioritize and handle multiple tasks
  • Excellent attention to details
  • Excellent knowledge of spoken and written English
Job Responsibility
Job Responsibility
  • Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality
  • Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with Procedural Documents, ICH-GCP and local regulations
  • Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality
  • Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks
  • Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study
  • Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations
  • Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in AZ clinical studies financial system by regular checks of the system and financial reports (as agreed with Director, SMM/ Director, Country Head
  • Ensures timely preparation of local Master CSA (including site budget) and amendments as needed
  • Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant SOPs and local regulations
  • Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with SOPs
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Read More
Arrow Right

Executive Director, Medicine Development Leader

GSK is seeking a highly skilled Executive Director, Medicine Development Leader ...
Location
Location
United States; United Kingdom , Waltham; London; Stevenage; Collegeville
Salary
Salary:
242250.00 - 403750.00 USD / Year
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree including MD, PhD, PharmD, MBA, MS
  • Drug development expertise in the global pharmaceutical/biotechnology industry
  • Filing experience with BLA/NDA/MAA submissions as a core responsibility
  • Experience in the entirety of drug development across the R&D/commercial life cycle including Discovery, late-stage Development, Regulatory, Manufacturing Medical and Commercial
  • Experience in product development and/or commercialization, in late phase development (from clinical PoC onwards), clinical trial management, post-approval studies, regulatory and manufacturing compliance
  • Experience leading teams in a complex, matrixed, global and multi-disciplinary organization with high accountability, minimal authority and multiple lines of reporting
  • Experience working with regulators and with regulatory requirements including legal and government frameworks within and across global geographies
  • Experience creating the strategy for pre- and post-marketing studies and driving the lifecycle process
  • Experience building budgets and leading the strategic and budget planning process
  • Experience the healthcare environment, and access in all major markets
Job Responsibility
Job Responsibility
  • Act as a single point of accountability in GSK for all aspects of a medicine being developed globally, from proof of clinical activity (POC) to Approval in all major market(s)
  • Work closely with the Early Development Lead (EDL) and Medicine Commercial Lead (MCL) to ensure a smooth transition of the lead indication(s) from the EDL upon achievement of clinical PoC and to the MCL upon Approval in first major market(s)
  • Post-approval, provide key support to the Medicine Commercial Team (MCT) in the first major markets ensuring the MDT provides optimal support to registration, including Post-Marketing Requirements (PMRs) and life cycle management (LCM) in the major markets
  • Work with the functional line Heads supporting RIIRU to select MDT members and lead this multi-disciplinary matrix team, supporting differentiated development for team members, owning the performance of the MDT and partnering with Line Managers to drive performance
  • Partner with the Pipeline Project Manager (PPM), energize and motivate the MDT to drive a high performing team and operational delivery of the project, including setting team objectives to ensure successful project delivery, including options for acceleration, parallel indication development and smart risk-taking.
  • Partner with R&D Business Development, leading the development planning for a prospective in-licensed asset by bringing together input from the relevant functions and TA experts to develop a Medicine Profile (MP) and development plans including but not limited to clinical feasibility, regulatory planning and CMC risk mitigation
  • Leads the cross-functional MDT to: Establish a compelling vision for the medicine and Target Medicine Profile (TMP) which positions the medicine within the R&D strategy taking the competitive landscape into account, translating GSK’s strategy into asset strategy and actionable plans for multiple areas or functions
  • Deliver differentiated medicines of value for patients, stakeholders and markets through an evidence package that supports regulatory approval, market access and the product’s life cycle
  • Prioritize and maximize the asset’s development options including developing multiple indications
  • Partner with the Global Medical Lead (GML) and MCL to develop an indication expansion and LCM plan for the asset.
What we offer
What we offer
  • Annual bonus
  • Eligibility to participate in our share based long term incentive program
  • Health care and other insurance benefits (for employee and family)
  • Retirement benefits
  • Paid holidays
  • Vacation
  • Paid caregiver/parental and medical leave
  • Fulltime
Read More
Arrow Right

Ptab gtm she lead

PTAB GTM SHE Manager has overall responsibility for managing Occupational Health...
Location
Location
Turkey , Istanbul
Salary
Salary:
Not provided
unilever.com Logo
Unilever
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s in Science/Engineering
  • Special studies in Supply Chain related subjects
  • 5 – 10 years in supply Chain operations
  • Advanced mentoring and coaching skills
  • Senior Stakeholder management skills
  • Advanced Project Management Skills
  • Good observation and auditing skills
  • University Science and Engineering degree qualification advantage
  • Experience in Supply Chain
  • Excellent knowledge of Unilever and SHE ISO standards
Job Responsibility
Job Responsibility
  • Defines and leads overall implementation of SHE strategy, priorities, and roadmaps for PTAB GTM in line with overarching Global and Regional level strategy and priorities to achieve excellent sustainable results. Identifies risks and effective strategies for mitigation in close collaboration with Categories SC and BO leadership
  • Provide efficient and long-standing Business Partnering: brings expertise, risk analysis, solutions, trainings and operational support to TR Board and PTAB GTM Critical Stakeholders. Implements License to Lead and other trainings to Leadership required to operate and lead Safety agendas with confidence
  • Supports and actively participates in business continuity and crisis management forums coordinating IMT (incident management team) activities action as a Coordinator. Coordinates delivery of capability trainings and technical support
  • Partners with the Regional and Category env capability teams (Env and Engineering) to drive initiatives towards env compliance and sustainability. Coordinates delivery of Sustainability Roadmaps to reduce Waste, Water, Energy and CO2 footprints in factories and Logistics
  • Works together with EU&PTAB SHE Director to secure line leadership commitment to help promote and embed safety into Business Agendas, personally promotes and leads by examples the culture of Safety Moments, Safety Behavior Observations on the shopfloor
  • Coordinates bi-monthly CSHEC (Central Safety Health and Env) committee meetings with TUI Supervisory Board acting as a Coordinator and Facilitator
  • Expertly supports PTAB Safe Travel (Road Safety) committee meeting. Leads regular follow up reviews to track implementation of agreed actions
  • Defines and deploys a comprehensive Communication Plan to promote safe behaviors in the organization at all levels based on identified risks and incident trend analysis
  • Coordinates risk assessment of sites and ensures adequate programs are deployed consistently to mitigate high risk activities related but not limited to Electrical Safety, Working @ Height, Process Safety, Permit to Work tasks, Construction Safety, Road Safety, MMHE. Enables implementation of Industrial Hygiene programs
  • Implements Safety standards and protocols towards 3P Collaborative Logistics partners, , logistical centers/ warehouses and transport haulers.
  • Fulltime
Read More
Arrow Right
New

User Experience Researcher, Qualitative

Our UX Research team is designing for businesses of all shapes and sizes, which ...
Location
Location
United States , Bellevue
Salary
Salary:
141000.00 - 192000.00 USD / Year
meta.com Logo
Meta
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree with 4+ years of relevant experience within user experience, applied research setting and/or product research and development, Master’s degree and 2+ years relevant experience, or a PhD and relevant experience
  • Experience conducting In-Depth Interviews or Focus Groups and Concept Testing or Usability Testing
  • Interest in and experience executing hands-on, primary research
  • Experience translating research findings into strategic narratives
Job Responsibility
Job Responsibility
  • Work closely with product and business teams to identify research topics
  • Act as a thought leader in the domain of research, while advocating for the people who could use our products
  • Design and execute end-to-end custom primary research using a wide variety of methods
  • Design studies that address both user behavior and attitudes
  • Effectively manage and prioritize research plans through ambiguous and fast-changing environments, align and efficiently execute critical insights and work with a large group of stakeholders
  • Communicate results and illustrate suggestions in compelling and novel ways
  • Work cross-functionally with design, product management, content strategy, engineering and marketing
  • Generate insights that both fuel ideation and evaluate designs
What we offer
What we offer
  • bonus
  • equity
  • benefits
  • Fulltime
Read More
Arrow Right
New

Welding Inspector

Reporting in to the Construction Superintendent, working as a Field Engineer / W...
Location
Location
United Kingdom , Bridgwater
Salary
Salary:
Not provided
assystem.com Logo
ASSYSTEM
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s or Master’s degree in Mechanical Engineering
  • Welding Inspector qualification (CSWIP 3.1 or equivalent)
  • NDT Appreciation qualification
  • Good working knowledge of Quality Management practices, methods and processes
  • Experience in punchlist checks and QA/QC activities
  • Knowledge of documentation used in safety‑critical construction and fabrication environments (e.g., Inspection and Test Plans, End of Erection Status Reports)
  • Knowledge of the fabrication and installation of pressure systems
  • Good knowledge of pipework, tanks/vessels, steelwork and heat exchangers
  • Broad knowledge and understanding of the engineering / construction industry including materials, trades, methods and legal requirements
  • Excellent organisation, delegation and communication skills
Job Responsibility
Job Responsibility
  • Verify that works are delivered in accordance with contractual requirements and notify the Construction Superintendent of any non‑conformance request needs
  • Provide details to support the issuing of non‑conformance reports
  • Maintain strong communication with all site teams and ensure surveillance activities are promptly reported
  • Contribute surveillance data to support KPI measurements
  • Identify potential quality issues early and support mitigation actions
  • Assist the team in implementing temporary measures to maintain safety and quality, and take proportionate follow‑up actions (e.g. issuing communications, arranging meetings)
  • Ensure design decisions are not made informally on site and are escalated through the proper approval process
  • Maintain awareness of current and upcoming site activities
  • Ensure tasks are delivered to required health, safety and environmental standards
  • Develop and maintain an understanding of construction drawings, activities, Quality Control Plans and Quality Inspection Records
What we offer
What we offer
  • 25 Days Annual Leave + Bank Holidays
  • Buy & Sell Holiday
  • 8% Company Pension Contributions
  • Income Protection & 3x Salary Death-in-Service Cover
  • Competitive Sick Pay
  • Healthcare Cash Plan – Claim back on dental, optical & more
  • Free Digital Gym Access – Expert-led fitness classes
  • Exclusive Discounts – Restaurants, days out & top brands
  • 24/7 Employee Support Line – Mental health, financial & legal help
  • Cycle to Work Scheme
  • Fulltime
Read More
Arrow Right
New

AI Research Scientist, Computer Vision - Facebook Video Intelligence

The Video Intelligence team is an applied AI research team within the Facebook p...
Location
Location
United States , Bellevue
Salary
Salary:
122000.00 - 181000.00 USD / Year
meta.com Logo
Meta
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Currently has, or is in the process of obtaining a Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience. Degree must be completed prior to joining Meta
  • PhD in Computer Science, Machine Learning, or a relevant technical field
  • Experience training multimodal, computer vision, LLM or related AI/ML models
  • Programming experience in Python and hands-on experience with frameworks such as PyTorch
  • Must obtain work authorization in the country of employment at the time of hire, and maintain ongoing work authorization during employment
Job Responsibility
Job Responsibility
  • Build a variety of multimodal foundation models such as text-to-video generative models, image-to-video generative models, video understanding models, unified native video generative models
  • Design core foundation model architectures and progressive pre-train
  • Post-train foundation models using techniques such as Supervised Fine-Tuning (SFT), Reinforcement Learning from Human Feedback (RLHF), Direct Preference Optimization (DPO), and Low-Rank Adaptation (LoRA)
  • Conduct research to develop SOTA GenAI models for the Facebook family of apps
What we offer
What we offer
  • bonus
  • equity
  • benefits
Read More
Arrow Right
New

Radiation Protection Consultant

As a Radiation Protection Consultant, you’ll play a pivotal role in ensuring the...
Location
Location
United Kingdom , Bridgwater
Salary
Salary:
Not provided
assystem.com Logo
ASSYSTEM
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PCN or equivalent ISO 9712 / ASME Level 2 Radiographer (current preferred
  • lapsed accepted)
  • Trained and previously appointed Radiation Protection Supervisor (RPS)
  • Strong understanding of IRR2017, CDM Regulations 2015, and Nuclear Site Licence conditions
  • Experience working on large construction, nuclear, or industrial sites with open-site radiography
  • Practical knowledge of radiographic barrier plans and coordination of field operations
  • Excellent communication and stakeholder management skills
  • Familiarity with national and international HSE standards
Job Responsibility
Job Responsibility
  • Coordinate radiography activities and interfaces between service providers and contractors to ensure safe and timely delivery
  • Manage radiographic film storage and support digitisation strategies for key component records
  • Champion non-radiological testing technologies to achieve ALARP (As Low As Reasonably Practicable) standards
  • Collaborate with Radiography SMEs and RPA bodies to review and approve ALARP justifications for innovative testing techniques
  • Conduct on-site safety monitoring, ensuring radiographic activities align with approved barrier plans
  • Track and analyse KPI performance, identifying trends, risks, and opportunities for improvement
  • Work closely with Health & Safety, Quality, and Regulatory teams to ensure full technical and legal compliance
  • Provide expert input into radiography strategy, risk management, and assurance processes
What we offer
What we offer
  • Pension scheme — 8% company / 4% employee contribution
  • 25 days’ annual leave + bank holidays + option to buy/sell
  • Flexible working options
  • Professional fees reimbursed
  • Employee referral bonus scheme
  • Income protection & 3x salary life assurance
  • Fulltime
Read More
Arrow Right
New

Network Operations Engineer

Meta is seeking a Network Operations Engineer to join our Edge and Network Servi...
Location
Location
United States , Denver
Salary
Salary:
159000.00 USD / Year ▼
meta.com Logo
Meta
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Currently has, or is in the process of obtaining a Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience. Degree must be completed prior to joining Meta
  • 4+ years of experience operating, deploying, and designing large-scale network, optical, and/or physical layer infrastructure
  • 4+ years of network operations experience while supporting large-scale service provider, data center, and/or enterprise network infrastructure
  • Hands-on experience with various optical/network communication equipment such as network/fiber/copper test gear, and other WDM equipment, as well as associated tools and test equipment
  • Communication skills with a demonstrated ability to engage effectively with hardware vendors, service providers, and colocation facility vendors globally, and translate performance issues into actionable technical requirements
  • Experience analyzing tactical situations, troubleshooting, root causing systems and tools, and problem solving via tasks or larger cross functional projects
  • Ability to provide technical guidance to external vendors to direct repair actions
  • Working knowledge of Network Services, including topology, traffic analysis, hardware platform, and architectures
  • Familiarity with Enterprise and Service Provider network hardware platforms and architectures, including Cisco and Juniper routers/switches and Nexus data center switching hardware platforms
  • Knowledge of physical data center design: rack elevations, cabling, fiber optics, power/cooling, and facility infrastructure
Job Responsibility
Job Responsibility
  • Incident Response: Collaborate with cross-functional teams, managed service providers, and third-party vendor partners to investigate complex technical and process issues during major incidents/site events (SEVs) on edge, caching, and network infrastructure. Work closely with team members to understand the root cause of incidents and contribute to their resolution
  • Change Management: Identify security & business continuity issues affecting the network and infrastructure at Meta and work with the team to implement effective changes. Provide feedback on existing tools, processes, and policies to help scale with the rapid expansion of the Meta platform and customer base
  • Operations: Drive operations by identifying improvement opportunities across policies, processes, and procedures to improve efficiency and quality of activities. Ensure standards compliance across the network and optimize service delivery
  • Collaboration and Partnership: Work closely with internal customers to address their needs and issues, and influence future iterations of data center and network designs for seamless integration of new infrastructure and scalability
  • Team Leadership: Work with cross-functional teams within and outside the organization to deliver business outcomes predictability across global sites. Analyze operational datasets to detect and prioritize problems and create aligned team projects, programs, and roadmaps
  • Risk Management: Collaborate with partner teams to design and implement aligned processes that identify and manage data and asset protection risks, as well as operations continuity issues across the network
  • Information and Data Assurance: Ensure relevant operational process, procedure, and policy documentation is effectively managed, and the data required to support operations is complete and accurate in systems
  • Automation: Collaborate with the team to analyze operational events to identify new automation opportunities and achieve our goals of all Tier-1 faults in the network being fully remediated by software. Help others understand our requirements and drive their roadmaps, and in some cases, directly implement lightweight solutions in code
  • Data Measurement: Drive quality into the metrics we report, measuring and analyzing escalation issues, fault/event trends, infrastructure capacity, and vendor performance failures. Formulate appropriate metrics and definitions of success to drive quality, efficiency, cost, and timeliness, evolving these over time to match changes to the infrastructure and business requirements
  • Communication: Provide clear and effective communication around personal and team goals, progress, outcomes, and lessons learned across assigned scope
What we offer
What we offer
  • bonus
  • equity
  • benefits
  • Fulltime
Read More
Arrow Right
Jobs by Category
Art and Entertainment Jobs Banking Jobs Call Center Jobs Construction Jobs Consulting Jobs Customer Service Jobs Education Jobs Energy Jobs Finance Jobs Gastronomy Jobs Health and Beauty Jobs Hospitality and Tourism Jobs Human Resources Jobs Insurance Jobs IT - Administration Jobs IT - Software Development Jobs Legal Jobs Logistics Jobs Manufacturing Jobs Marketing, Digital Marketing, SEO, SEM Jobs Media Jobs Nursing Jobs Office Administration Jobs Pharmacy Jobs Physical Work Jobs Public Relations Jobs Public Sector Jobs Purchasing Jobs Quality Control Jobs Real Estate Jobs Research and Development Jobs Sales Jobs
Job Positions Jobs by Country
United States Jobs United Kingdom Jobs India Jobs Canada Jobs Australia Jobs Germany Jobs Ireland Jobs Poland Jobs
Company
Blog About Us Contact
Follow Us
Facebook
X (Twitter)
LinkedIn
Instagram
CrawlJobs Group
ITFlashcards AllDevBlogs
© 2026 CrawlJobs Ltd. All Rights Reserved
Terms & Conditions Privacy Policy