İş Yeri: Warsaw, Bangalore, UK - Hertfordshire - Stevenage
Yayın tarihi: Feb
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.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
* 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.
Why You?
Working arrangement
This role is hybrid. You will be expected to work regularly from our office and collaborate with international colleagues.
We are seeking professionals with the following required skills and qualifications to help us achieve our goals
* 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.
If you have the following characteristics, it would be a plus
* 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 you will bring
* Attention to detail and a disciplined approach to documentation and follow-up.
* A problem-solving mindset that looks for practical and sustainable solutions.
* Strong interpersonal skills to build working relationships across clinical, quality and operational partners.
* Integrity and a focus on patient safety and data integrity.
* Willingness to learn, adapt and take on new responsibilities to grow your career.
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.
We're looking for someone who thrives in a collaborative environment, is passionate about delivering results, and is eager to make a difference. If this sounds like you, we'd love to hear from you
#LI-GSK
#LI-HYBRID
The annual base salary in Poland for new hires in this position ranges from PLN 168,000 to PLN 280,000 gross, taking into account a number of factors including the candidate's skills, experience, education level and the market rate for the role. Depending on the role and internal policies, the position may also be eligible for a bonus (if applicable and based on defined, non-discretionary criteria) and/or awards for exceptional performance (granted at the employer's discretion). All statutory benefits will be maintained in accordance with Polish law. Other benefits may also be offered, which may include private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave & care of family member leave.
More detailed information on the total reward package applicable to your role will be supplied during the recruitment process. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the market rate for the role.
As an Inclusive employer, we encourage you to reach out if you need any adjustments during the recruitment process. Please contact our Recruitment Team at pl.recruitment- to discuss your needs.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website