Mapi Group

Werken bij Mapi Group

Mapi Group

Soort organisatie
Aantal medewerkers
Internationaal actief

Wie zijn wij?

Mapi is a leading global organization, offering evaluation and support of therapeutic strategies. With offices worldwide, Mapi provides high quality and efficient operations to help our clients secure product approvals and reimbursement, as well as addressing post-clients (pharmaceutical, biotech, medical device and vaccine companies) marketing requirements and late phase needs, meeting the needs of patients, physicians, regulatory authorities and health care technology purchasers.

Mapi has an excellent reputation in evidence-based health research due mainly to the quality of our people and deliverables. As such we provide a dynamic, stimulating and rewarding working environment for ambitious and passionate individuals looking to join a global, world-class consultancy business. 

Plan route



Clinical Research Associate, Late-Phase, Real World Evidence
As Clinical Research Associate, Late Phase at Mapi Group, you will be responsible for performing all monitoring and site management activities within the monitoring and site management (MSM) team. You will perform routine site visits to ensure that the rights and well-being of human subjects are protected; the trial data is accurate, complete, and verifiable from source documents. You will ensure that all activity is delivered in accordance with the study protocol, GCP/ICH/GEP guidelines and applicable regulatory requirements.ResponsibilitiesPerform site feasibility and site selection in conjunction with Site Management Associates, or independently.Work closely with relevant departments to perform Regulatory and IEC/IRB submissions and contract negotiationsPerform site and remote visits including pre-study, site initiation, interim and close out to monitor informed consent procedures, compliance protocol, GCP/ICH guidelines and other applicable regulatory requirementsContribute to and where necessary lead; sponsor or regulatory site audits/inspections including preparation , attendance and follow-up audit findingsMaintain regular site contacts to ensure site compliance, enrolment and understanding of study requirementsMaintain the Project Tracking System recording site visit dates, site contact notes, subject and site informationWrite and review project plans and templatesAssist with the development of departmental and project specific processes and proceduresKnowledge, Skills and AttributesStrong knowledge of ICH/GCP guidelines and/or other relevant guidelines (GEP, GPP) and local requirements (including regulatory)Proficiency with computer/software systemsProven ability to project manage multiple simultaneous tasksFor non-native English speakers; possess strong written and verbal English skillsEducationThree (3) year degree preferably in a scientific, medical or life sciences discipline or considerable relevant practical and professional experienceClinical Research Certification is highly desiredWhat will you get?Values: At Mapi, we embrace our values, and everyone that works here is expected to demonstrate these values and associated behaviours in their day-to-day work. Our values are the foundation of the work we do, and include ownership, transparency, fairness, adhere to beliefs, adaptation, empathy and sincerity….to name but a few.Culture: We promote personalisation as part of our culture, where each individual has a voice and can be heard. Our teams are diverse, multicultural and experts in their own field. To fit in culturally at Mapi, you will need to believe in and evoke our values.At Mapi, we are committed to improving the quality of patient care worldwide. We do this by offering strategic and insightful solutions for successful market access to people who are shaping tomorrow’s health care. Our values serve as the guiding principles in fulfilling our commitments to the patient and to our clients. 30+ dagen geleden

Mapi Group
Bargelaan 200
2333CW Leiden

dkerrigan (mapigroup)

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