Senior Clinical Research Associate - Sponsor dedicated - Belgium - Home based (m/w/d)

IQVIA; Zaventem; Hybrid; EUR 50,000 - 70,000; Full time

Benefits offered by this job

Company car

Mobile phone

Attractive rewards and benefits package

Job summary

IQVIA LLC in Zaventem, Belgium, is seeking a motivated Senior Clinical Research Associate to join our dynamic Sponsor dedicated model. This role involves performing site monitoring visits and ensuring compliance with protocols while collaborating effectively with site investigators.

Ideal candidates will hold a relevant university degree, possess over 3 years of monitoring experience, and be fluent in Dutch, French, and English. Join us for growth in a successful global organization with a supportive culture and benefits package.

Qualifications

• Minimum of 3 years of independent, on-site monitoring experience as a CRA.
• Good knowledge of clinical research regulatory requirements.
• Strong ability to build trusted partnerships with site investigators.

Responsibilities

• Perform site monitoring visits and ensure compliance with protocols.
• Track regulatory submissions, recruitment, and case report form completion.
• Create documentation regarding site management and monitoring findings.

Skills

Excellent communication skills in Dutch, French, and English

Organizational and problem-solving skills

Interpersonal and cross-cultural communication skills

Knowledge of Good Clinical Practice (GCP)

Independent on-site monitoring experience

Education

University degree in scientific discipline or health care

Job description

## Senior Clinical Research Associate - Sponsor dedicated - Belgium - Home based (m/w/d)Applylocations: Zaventem, Belgiumtime type: Full timeposted on: Posted Todayjob requisition id: R1555460Internal Job DescriptionIQVIATM is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients.Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.Within our Sponsor dedicated model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are ‘indication and molecule experts’. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study.Leadership recognises the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows. Our managers understand the sponsors priorities and the individual aspects of each model. Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development.Additionally, IQVIA’s sponsor dedicated business works with the Sponsors SOP’s, creating more continuity for both parties.Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills.IQVIA Belgium are currently seeking **motivated Senior Clinical Research Associate** practitioner to join our unique and dynamic Sponsor dedicated model.This is a role **based in Belgium*****Your Role:**** Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines* Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.* Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.* Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.* Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.* Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.* Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.* Collaborate and liaise with study team members for project execution support as appropriate.* If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.***Your Profile:**** **University degree in scientific discipline or health care*** **Minimum of 3 years of independent, on-site monitoring experience** as a CRA within a CRO or pharmaceutical environment.* **Excellent communication skills in Dutch, French, and English, both written and spoken.*** Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Organizational and problem-solving skills.* Exceptional interpersonal and cross-cultural communication skills to build strong, trusted partnerships with Belgium site investigators and medical staff.* A collaborative mindset to work effectively with cross-functional global teams, project managers, and local study coordinators.***Why join us?**** Grow your career with access to development resources, training, and advancement opportunities* Enjoy the flexibility and trust to balance your professional and personal commitments* Expand your therapeutic knowledge through dedicated learning and development programs* Be part of a successful global organization with an excellent reputation and supportive culture* Benefit from a company car, mobile phone, and an attractive rewards and benefits packageIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.