Clinical Research Specialist

# Clinical Research SpecialistJohnson & Johnson Machelen 3 maandenGepubliceerd 10 uur geleden
· Opportunity ID: 1059996Tarief indicatie —Uren 40 u/wStart 30 Nov 2026Duur 3 maandenInteresse in deze opdracht?## De opdrachtSenior Clinical Research SpecialistLocation: This role will require a large amount of travel across the EU. Base site will be Diegem on a hybrid basis Duration: 1 yearHours: 40 hours per week (100%)Imagine your next project as a Senior Clinical Research Specialist, working at the forefront of cutting edge work and technology with one of the leading Pharmaceutical companies in the worldroles and responsibilities
- Serves as a Senior Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, for Johnson&Johnson MedTech Electrophysiology;
- Oversees/executes feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures;
- May serve as the primary contact for clinical trial sites (e.g. site management);
- Contributes towards development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports,....);
- Supports applicable trial registration from study initiation through posting of results and support publications as needed;
- Manages/oversees ordering, tracking, and accountability of investigational devices and trial materials;
- Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel;
- Interfaces, collaborates and oversees Clinical Research Associates (CRAs);
- Oversees and supports the development and execution of Investigator agreements and trial payments;
- Is responsible for clinical data review to prepare data for statistical analyses and publications;
- May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need;
- May contribute to the development and delivery of appropriate global evidence generation strategies (EGS) and evidence dissemination strategies (EDS) within the assigned projects;
- May provide on-site procedural protocol compliance and data collection support to the clinical trial sites;
- Contributes to the critical assessment of the literature and to the interpretations and disseminations of all evidence generated;
- Contributes to delivery of assigned clinical projects, through effective partnership with the study core team leading to delivery of clinical project commitments (deliver on time, within budget and in compliance with regulations and SOPs);
- May assist with the development of e Post-Market Clinical Follow-up (PMCF) Plans and PMCF Evaluation Reports (ER) within the defined timelines and review/update at planned intervals; May assist with maintaining the overview to assure (study) commitments are timely and properly met by coordination of specific documentation and contribution to cross-functional review of associated documents where relevant;
- Supports project/study budget activities;
- Mentors team members;
- Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders;
- Should develop a strong understanding of the pipeline, product portfolio and business needs;
- Generally manages work with supervision, dependent on project complexity. Independent decision-making for simple and more advanced situations but requires guidance for complex situations.
- Responsible for communicating business related issues or opportunities to next management level;
- Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable;
- For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable;
- Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures;
- Performs other duties assigned as needed;
- May act as Clinical Safety Coordinator:

Requirements:
- Minimum of a Bachelor’s Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.
- BS with at least 4 years, MS with at least 3 years, PhD with at least 2 years of relevant experience preferred.
- Strong experience in the development of clinical trial documents (e.g. study protocol, informed consents,
- Previous experience in clinical research or equivalent is required.
- Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR, MEDDEV,...).
- Good understanding of clinical research science and processes, clinical tr