Daily new jobs


Senior Clinical Study Manager

Delen op Social Media:

Solliciteer Bewaar deze vacature

1 persoon heeft ook gesolliciteerd op deze vacature

The company

Our client is a professional Medical Devices organisation, based in Noord-Holland Netherlands. International Medical Devices Company with over 300 products for among others cardiology and orthopedics.

Role description

This position is responsible for providing project management and leadership to plan, prepare and execute multiple clinical projects. Internally interfaces with data management, clinical research associates, Quality, Regulatory, and functional management. Acts as liaison with external customers including site investigators,
clinical site staff, vendors, and medical and scientific personnel. Accountable for timeline development, communication, and accountability of study outcomes and milestones to internal and external customers.


1. Design, implement, manage, and terminate clinical trials.
2. Manage clinical studies and ensure they are carried out in accordance with the Protocols, Good Clinical Practices (GCP's), Standard Operating Procedures (SOP's) and other regulatory requirements.
3. Collaborate in the development, approval, and distribution of study-related documents including study protocols, informed consent documents, study plans, study manuals, and other study tools to investigational sites and review committees.
4. Prepare and participate in presentation of protocols and other study requirements at study initiations at investigational sites when needed.
5. Must have the ability to monitor on-going compliance to study protocols and site adherence to global regulatory guidelines.
6. Oversee subject screening and enrollment at assigned clinical sites, track enrollment.
7. Manage the distribution, collection and tracking of regulatory documentation to ensure compliance at both the sites and Sponsor Central File, and for audit readiness.
8. Assist in the planning, preparing, and distributing of materials for investigator and coordinator meetings, and for study related training.
9. Track and report progress of studies including patient enrollment/screening, patient accountability, device accountability, etc.
10. Oversee vendor management activities as needed, including the Request for Proposal and vendor selection and contracting activities.
11. Provide mentoring to junior staff regarding protocols and site management.
12. Assists data management with the development and review of Case Report Forms for content and ensure proper data is provided for their input analysis and output of reports.
13. Prepare and provide timely reports to management.
14. Assist in the development and management of study budget.
15. Maintain registrations on Clinical trial.gov.
16. Review Monitoring Trip Reports provided by Field Monitors.
17. Select and qualify clinical trial investigational sites, including managing aspects related to physician relationships, and manage IRB/EC approvals (initial and ongoing).
18. Assist in the distribution of investigational product.
19. Participate in the development and implementation of internal policies & procedures to optimize management of clinical trials; contribute to process improvement.
20. Oversee and participate, as needed, in site close-out visits, report reviews, and follow-up to resolve final site issues.
21. Work with Regulatory Affairs as needed to provide accurate and timely reports, such as annual reports or safety reports to the FDA and other regulatory bodies.


Identify specific technical skills and competencies (for example: work environment/safety, quality, customer focus, results focus, sense of urgency, initiative, leadership, etc.)
• Solid understanding of the clinical study process, preferably of medical devices.
• Proficient working knowledge of the regulations (Food and Drug Administration (FDA), Good Clinical Practice (GCP), International Committee on Harmonization (ICH), ISO, etc).
• Organizational awareness to operate in cross-functional teams and provide leadership to other clinical staff members.
• Effective communication and time management skills required.
• Must commit to work in a safe environment that is quality- and customer-focused.
• Must recognize and commit to a sense of urgency, teamwork.
• Must be able to take and maintain initiative.
• Possess strong interpersonal skills with the ability to interact with peers, medical professionals, consultants, and Regulatory Agencies as required.
• Must be able to plan, problem solve with the use of critical thinking skills.

Other information

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ewout de Jong.

Job alert

  • Geen registratie nodig
  • Blijf op de hoogte van de nieuwste vacatures

SIRE Life Sciences®

Geplaatst door: SIRE Life Sciences®
Geplaatst op: 03-06-2019
Land: The Netherlands
Regio: Noord-Holland
Dienstverband: Permanent
Expertise: 3 - 5 jaar
Locatie Type: Op locatie
Opleiding: Master
Taal: Engels
Sector: Medical Devices
Specialisatie: Clinical

Opnieuw zoeken

Gerelateerde vacatures

Ewout de Jong
Longterm project: Compliance Specialist

The Netherlands

Ewout de Jong
On site Quality Specialist

The Netherlands

Ewout de Jong
Quality Assurance Specialist Orthopedics

The Netherlands

Ewout de Jong
QA Complaint Handling Specialist

The Netherlands

SIRE Information Technology®
Quality Engineer for a contractor in the Oil&Gas industry

The Netherlands


SIRE Life Sciences B.V.

Mondriaan Tower
Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 20 658 9800

SIRE Life Sciences Deutschland GmbH

Fünf Höfe
Theatinerstraße 11
80333 München
+49 (0) 89 3803 8966

SIRE Life Sciences UK

702 Howard House Dolphin Square
SW1V3PQ London
+44 7307 179882

SIRE Staffing Solutions B.V.

Keizersgracht 440A
1016 GD Amsterdam
+31 (0) 20 658 9804

SIRE Life Sciences Consultancy B.V.

Wetenschapsstraat 14B
1040 Bruxelles
+32 (0) 2 588 1277