Check out this great opportunity at a leading medical devices company ! You have a solid experience within clinical trials, able to work in an independent manner, and you are looking for a broad, varied job within a dynamic medical devices company ? Then check out this opportunity. Our medical devices client is looking out to reinforce their clinical team with a motivated and enthusiastic Clinical Research Specialist. Triggered ? Don't hesitate and apply today !
Hybrid working opportunity at client's location in Belgium.
The Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization.
- Serves as a Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones.
- 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 (e.g. www.clinicaltrials.gov) 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;
- May act as Clinical Safety Coordinator
- Mentors team members;
- May perform other duties assigned as needed;
- Is responsible for communicating business related issues or opportunities to next management level.
- Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders;
- Is responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures;
- 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.
- 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.
- 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,…).
- Clinical/medical background is a plus.
- Medical device experience is highly preferred.
- Good understanding of clinical research science and processes, clinical trends, and global clinical trial regulations;
- Proven track record in supporting delivery of clinical projects within clinical/ surgical research setting, on time, within budget and in compliance to SOPs and regulations;
- Good presentation and technical writing skills;
- Good written and oral English communication skills;
- Ability to lead small study teams to deliver critical milestones, as may be assigned.
- Existing right to work in Europe is required
- A balanced salary package based on your capabilities and experience, including extra-legal benefits
- Hybrid working opportunity (50/50)
Vacancy number: 23429