CrawlJobs Logo

Clinical Compliance & Improvement Associate

us.gsk.com Logo

GSK

Location Icon

Location:
Poland , Warsaw

Category Icon
Category:
Pharmacy

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

168000.00 - 280000.00 PLN / Year
Save Job
Save Icon
Apply Position

Job Description:

You will join the Clinical Compliance & Improvement (CCI) team to support clinical compliance, early issue detection and continuous improvement across Development Operations. You will work with colleagues in clinical teams, quality, and operations to gather data, perform compliance monitoring activities, and help deliver practical solutions. We value clear thinking, attention to detail, a collaborative mindset, and curiosity. This role offers strong learning and development, real influence on how trials are run, and the chance to help ensure patient safety and data integrity as we unite science, technology and talent to get ahead of disease together.

Job Responsibility:

  • Support compliance monitoring activities to detect trends, signals and emerging operational risks across assigned clinical teams
  • Help carry out compliance checks, management monitoring and follow-up activities to confirm corrective actions are effective
  • Collect, analyze and present compliance data and insights to inform improvement plans and priorities
  • Assist with issue governance activities including logging, tracking, escalation and communication of actions and outcomes
  • Support inspection and audit readiness activities by preparing documentation, responses and evidence as required
  • Contribute to continuous improvement projects, including data collection, root cause analysis and small project management tasks

Requirements:

  • Degree in a life science, pharmacy, nursing, clinical research or related discipline, or equivalent experience
  • 1–5 years’ experience in clinical operations, quality, compliance, or a related function
  • Practical knowledge of Good Clinical Practice (GCP) and clinical trial conduct
  • Experience working with data to identify trends, signals or process gaps
  • Good written and verbal communication skills in English
  • Able to work in a hybrid model with regular time in the local R&D office

Nice to have:

  • Experience supporting regulatory inspections or internal audits
  • Familiarity with clinical quality systems, issue management tools, or study oversight processes
  • Experience with root cause analysis and implementing corrective and preventive actions
  • Comfort working across multiple teams and stakeholders in a matrix environment
  • Proficiency with data analysis tools (Excel, Power BI, Artificial Intelligence, visualization tools), and clear reporting skills
  • Familiarity with clinical systems such as Veeva
  • Prior experience in a pharmaceutical or contract research environment
What we offer:
  • Performance with Choice – flexibility in working mode (hybrid working model 2/3 days per week in the office), flexible working hours
  • Established job in an international, well-known pharmaceutical company
  • Opportunity to work in professional team plays crucial role in maintaining GSK portfolio on the markets
  • Opportunity to work within GSK standards and documentation applied globally
  • Wide range of benefits (Medical Plan, Life Insurance, Employee Retirement Program, Sport and recreation cards, Recreation allowance, annual bonus)
  • Supportive & friendly working environment
  • 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:
February 21, 2026

Employment Type:
Fulltime
Work Type:
Hybrid work
Icon
GSK - 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 Clinical Compliance & Improvement Associate

Clinical Trial Operations Associate

Beacon Biosignals is on a mission to revolutionize precision medicine for the br...
Location
Location
United States , Boston
Salary
Salary:
Not provided
beacon.bio Logo
Beacon Biosignals
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experience in clinical project management or clinical operations roles
  • Strong organizational and project management skills, with the ability to manage multiple responsibilities effectively
  • Excellent written and verbal communication skills in English
  • A proactive mindset with the ability to identify priorities and anticipate challenges
  • Meticulous attention to detail, ensuring accuracy in data collection and reporting
  • Familiarity with GCP, ICH guidelines, and clinical research regulatory requirements
  • A desire to learn more about analytics, statistics, machine learning, and clinical trials
Job Responsibility
Job Responsibility
  • Collaborate with project teams to support study startup activities
  • Act as the primary point of contact for clinical sites, ensuring smooth operations and clear communication
  • Provide training to research sites on the use of Beacon’s devices and study protocols, ensuring proper device usage and data collection
  • Monitor project progress, ensuring adherence to timelines, protocols, and quality standards
  • Maintain compliance with Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and regulatory standards
  • Address operational issues promptly, escalating through tools like Zendesk and Asana for resolution
  • Provide actionable feedback from research sites to inform improvements in devices and workflows
What we offer
What we offer
  • equity
  • PTO
Read More
Arrow Right

Associate Vice President, Clinical Data Management

The Associate Vice President, Clinical Data Management is a member of the Global...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s or master’s degree with 25+ years of data management experience
  • 10 to 15 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources
  • Experience within clinical data management, regulatory compliance, and strategic leadership within a pharmaceutical, biotech, or CRO environment
  • Expertise in GCP, ICH, FDA, EMA regulations, data governance, and clinical trial data standards (CDISC, SDTM)
  • Experience within cross-functional collaborations, leadership, and strategic planning skills, ensuring operational excellence and compliance while driving innovation in data management to support Amgen’s global clinical development efforts
  • Expertise in AI/ML-driven data management solutions, automation, and advanced analytics
  • Understanding of clinical data standards (CDISC, SDTM, ADaM)
  • Experience leading regulatory submissions, including NDA/BLA/MAA filings and advisory committee interactions
  • Proven ability to drive organizational change, optimize processes, and implement lean principles in clinical data management
  • Cross-functional collaboration experience with clinical operations, regulatory affairs, biostatistics, and R&D teams
Job Responsibility
Job Responsibility
  • Develop and drive the global data management strategy in alignment with clinical development objectives and corporate goals
  • Provide strategic and operational leadership to the Clinical Data Management (CDM) function across all clinical programs and phases
  • Lead innovation initiatives, including the implementation of development integration programs and the adoption of cutting-edge technologies to enhance data workflows
  • Represent Clinical Data Management in executive leadership discussions, regulatory interactions, and industry forums
  • Establish and enforce robust clinical data governance models, policies, and risk mitigation strategies to ensure quality and compliance
  • Make final decisions regarding standard operating procedures (SOPs), CDM best practices, and process optimization
  • Engage key stakeholders and ensure timely resolution on critical data integrity and regulatory compliance issues
  • Serve as the primary CDM representative during regulatory inspections and audits, with responsibility for final decisions on findings, responses, and corrective actions
  • Influence cross-functional clinical development, operational, and regulatory strategies through data-driven insights and analytics
  • Partner closely with Clinical Program Operations, Regulatory, Biostatistics, and R&D to ensure seamless integration and alignment of clinical data
Read More
Arrow Right

Associate Counsel

Help drive Big Health’s growth by providing practical, business-minded legal sup...
Location
Location
United States
Salary
Salary:
125000.00 - 145000.00 USD / Year
bighealth.com Logo
Big Health
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • J.D. from an accredited U.S. law school and active membership in good standing with at least one U.S. state bar (California, Massachusetts, or Delaware preferred)
  • 3–5 years of relevant legal experience, ideally with a mix of law firm and in-house in healthcare, digital health, or life sciences
  • Strong experience drafting, reviewing, and negotiating a wide range of commercial contracts
  • Working knowledge of healthcare regulatory frameworks, including FDA regulations for software-based medical devices, HIPAA, and federal and state fraud and abuse laws
  • Familiarity with data privacy and security laws (e.g., HIPAA, GDPR, CCPA) and experience operationalizing privacy compliance
  • Ability to interpret and apply healthcare and data protection regulations in a practical, business-enabling manner
  • Strong written and verbal communication skills, with the ability to translate complex legal concepts and tailor messaging for varied, cross-functional audiences
  • Excellent organizational skills, attention to detail, and ability to manage multiple priorities in a fast-paced, high-growth environment
  • Comfort working cross-functionally with product, compliance, commercial, and regulatory teams
  • Proactive, solutions-oriented, and comfortable exercising sound judgment in ambiguous situations
Job Responsibility
Job Responsibility
  • Draft, review, and negotiate a variety of commercial and clinical contracts, including licensing, collaboration, research, and vendor agreements
  • Manage redlines, coordinate with internal stakeholders, and ensure alignment with regulatory, privacy, market access, sales, and other departments’ requirements
  • Maintain and improve contract templates and related policies and procedures to support deal cycles
  • Advise on compliance regarding healthcare regulations (e.g., Anti-Kickback, Sunshine Act, etc.), product claims and advertising, and data privacy laws (US and global)
  • Act as the first point of contact for day-to-day legal questions and translate complex laws into practical guardrails for business teams
  • Contribute to the development of scalable legal workflows and policies
What we offer
What we offer
  • generous vacation policy
  • professional development fund
  • flexible working arrangements
  • stock options
  • Fulltime
Read More
Arrow Right

Associate Director Biostatistics

Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN)...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate in Statistics/Biostatistics (or related subject with high statistical content) with at least 12+ years of post-graduate statistical experience in the pharmaceutical industry or medical research
  • Master’s degree in Statistics/Biostatistics (or related subject with high statistical content) with at least 16+ years of post-graduate statistical experience in the pharmaceutical industry or medical research
Job Responsibility
Job Responsibility
  • Provide sound statistical guidance to clinical development, reimbursement, and medical affairs
  • Oversee statistical contributions to protocols, randomization specifications, statistical analysis plans (SAPs), clinical study reports (CSRs), and key trial documents
  • Ensure alignment of study design and analysis with scientific rigor, regulatory requirements, and Amgen policies
  • Collaborate cross-functionally with global teams to deliver high-quality analyses, publications, and regulatory filings
  • Contribute to innovative trial designs, advanced methodologies, and process improvement initiatives
  • Execute biostatistical strategies across the product lifecycle, from early development through post-marketing
  • Provide consultancy and training to colleagues across R&D
  • Support governance of outsourced statistical activities, ensuring adherence to Amgen standards and regulatory compliance
  • Represent Biostatistics in cross-functional and external interactions (e.g., with regulatory agencies, investigators, or data monitoring committees)
  • Drive technology adoption leveraging AI capabilities to streamline statistician’s work
What we offer
What we offer
  • Vast opportunities to learn and develop within our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
Read More
Arrow Right

Business Development Associate

This role is responsible to drive sales, expand market share and increase produc...
Location
Location
Singapore
Salary
Salary:
Not provided
avanos.com Logo
Avanos
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Candidate with Nursing, Biomedical, Biotechnology or Science background preferred
  • At least 5 years of experience in related experience
  • Track record of profit/margin maximization, revenue growth, execute programs, manage projects and campaigns
  • Possess product training experience to clinical users and distributors
  • Strong understanding and identification of customers and their needs, clinical environment, competitive landscape and trends
  • Experience creating clinical acceptance and drive adoption of new treatments/therapies/technologies
  • Broad-based knowledge of medical consumables sales and marketing processes
  • Highly self-motivated, results-oriented with a drive and passion to succeed
  • Exceptional people skill and customer service oriented
  • Good communication and presentation skills
Job Responsibility
Job Responsibility
  • Drive sales, expand market share and increase product branding and awareness for the Company’s best-in-class products and business in assigned markets within Central Asia, mainly in Singapore
  • Participate in clinical cases, cadaver workshops and conferences
  • Perform equipment in-service maintenance and monitoring
  • Deliver product trainings to internal and external stakeholders e.g. sales team, physicians, clinical users, distributors, etc. to ascertain a solid understanding of AVANOS products, relevant technologies and application
  • Support operating procedures in the hospitals
  • Work closely with the Business Development Manager, Central Asia, ASEAN Sales Team, APAC Marketing Team to ensure the alignment of global, regional and local strategies, with the aim to elevate the company’s brand and improve product adoption efficacy through driving demand, sales and market expansion in the assigned markets
  • Work closely with cross-functional teams to own and drive customer satisfaction, product compliance, innovation and margin improvement
  • Be responsible for leading and building the Avanos Pain business mainly in Singapore
  • Achieve and exceed regional sales and financial budget and operational objectives
  • Drive growth on strategic focus products via increasing brand awareness and customer loyalty to Avanos products
What we offer
What we offer
  • Comprehensive and competitive range of benefits
  • Total Rewards package encompasses everything you receive as an employee
  • your pay, health care benefits, retirement plans and work/life benefits
Read More
Arrow Right

Brazil Country Head, Global Site & Study Operations Associate Director

Provide strategic and operational leadership for all study and site execution wi...
Location
Location
Brazil , São Paulo
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate degree and 3 years of clinical execution experience
  • Master’s degree and 7 years of clinical execution experience
  • Bachelor’s degree and 9 years of clinical execution experience
  • At least 3 years’ experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources
  • +8 years’ work experience in life sciences or medically related field, including 6 years of biopharmaceutical clinical research experience
  • Experience at, or oversight of, clinical research vendors (CRO’s, central labs, imaging vendors, etc.)
  • Significant experience managing clinical operations across relevant geography / region, including strong understanding of local regulatory requirements around global clinical trials
  • Advanced English proficiency
Job Responsibility
Job Responsibility
  • Provide strategic and operational leadership for all study and site execution within the assigned country or hub-and-spoke geography
  • Accountable for end-to-end study, site, and site engagement execution across the assigned country or hub-and-spoke geography
  • Provide strategic leadership for country commitments, acting as a key advisor on study feasibility, placement, and site selection
  • Lead, line-manage, and develop the Country/Hub team
  • Ensure adequate and timely resourcing across study delivery, site operations, and monitoring roles
  • Drive site engagement through a clearly differentiated Amgen site experience
  • Oversee country-level financial and operational management, including budgets, forecasting, vendor oversight
  • Lead country governance and risk management, including chairing the Country Management Team (CMT)
  • Ensure regulatory compliance, inspection readiness, and continuous improvement
What we offer
What we offer
  • Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans and bi-annual company-wide shutdowns
  • Flexible work models, including remote work arrangements, where possible
  • Fulltime
Read More
Arrow Right

Clinical Trial Operations Associate

Beacon Biosignals is on a mission to revolutionize precision medicine for the br...
Location
Location
United States , Boston
Salary
Salary:
Not provided
beacon.bio Logo
Beacon Biosignals
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experience in clinical project management or clinical operations roles
  • Strong organizational and project management skills, with the ability to manage multiple responsibilities effectively
  • Excellent written and verbal communication skills in English
  • A proactive mindset with the ability to identify priorities and anticipate challenges
  • Meticulous attention to detail, ensuring accuracy in data collection and reporting
  • Familiarity with GCP, ICH guidelines, and clinical research regulatory requirements
  • A desire to learn more about analytics, statistics, machine learning, and clinical trials
Job Responsibility
Job Responsibility
  • Collaborate with project teams to support study startup activities
  • Act as the primary point of contact for clinical sites, ensuring smooth operations and clear communication
  • Provide training to research sites on the use of Beacon’s devices and study protocols, ensuring proper device usage and data collection
  • Monitor project progress, ensuring adherence to timelines, protocols, and quality standards
  • Maintain compliance with Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and regulatory standards
  • Address operational issues promptly, escalating through tools like Zendesk and Asana for resolution
  • Provide actionable feedback from research sites to inform improvements in devices and workflows
What we offer
What we offer
  • equity
  • PTO
Read More
Arrow Right

Director Clinical Services

The Director, Clinical Services is responsible for the planning, direction, coor...
Location
Location
United States , Lexington
Salary
Salary:
42.99 - 63.95 USD / Hour
americannursingcare.com Logo
American Nursing Care
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Current RN license (BSN preferred), Physical Therapist license, or Occupational Therapist license in good standing
  • CPR or BLS certification (current)
  • Three years of management experience required
  • Two years of home care or hospice experience required
  • one year in hospital nursing preferred
Job Responsibility
Job Responsibility
  • Mission & Values Adherence: Champion CHI Health at Home and CommonSpirit Health's mission, values, strategic goals, and high standards of customer service
  • Ethical Conduct & Compliance: Uphold the Corporate Compliance Program
  • Operational Support: Provide prompt and professional assistance to office and clinical staff
  • Quality Care Oversight: Direct the accurate, complete, and timely provision of quality patient care and services, ensuring individualized patient plans of care are appropriate and in compliance with all regulatory, operational, and financial requirements
  • Clinical Record Compliance: Assure the accuracy, completeness, and timeliness of all clinical records, meeting regulatory, operational, and financial requirements
  • EMR Workflow Completion: Guarantee that all HCHB clinical workflow for both the Director of Clinical Services (DCS) and Manager of Clinical Services (MCS) is completed and current by the end of each business day
  • Outcome Monitoring & Improvement: Monitor clinical outcome results (utilizing SHP and company data), develop, and implement plans for continuous improvement
  • Clinical Performance Management: Monitor and evaluate clinical performance measures, including productivity standards, documentation completion standards, and patient care management, developing and implementing action plans based on results
  • Clinical Documentation Expertise: Ensure the ongoing development of clinical employee knowledge, understanding, and appropriate completion of OASIS, initial and ongoing physician orders, and all other clinical documentation tools
  • Information Dissemination: Ensure accurate, complete, and timely communication of regulatory, operational, and financial information to clinical and applicable office associates
What we offer
What we offer
  • Generous annual bonus opportunity based on company performance
  • Excellent holiday and paid time off plans
  • Medical, dental, and vision plans
  • Tuition reimbursement for degree-seeking students
  • Employer contribution to your 401(k)
  • Fulltime
Read More
Arrow Right
Remote jobs 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 Salaries About Us Contact
Follow Us
Facebook
X (Twitter)
LinkedIn
Instagram
CrawlJobs Group
ITFlashcards AllDevBlogs
© 2026 CrawlJobs Ltd. All Rights Reserved
Terms & Conditions Privacy Policy