Marcel De Ridder Email & Phone Number

Wijk Bij Duurstede, UT, NL

Amersfoort, Utrecht, Nederland

• Activities/responsibilitiesContracts:
• Responsible for coordinating and controlling contracts and other legal documents for clinical operations, communicating updates, and documenting activities in accordance with GSK SOPs and local legislation in-country.
• Accountable for negotiation and… Show more Activities/responsibilitiesContracts:
• Accountable for negotiation and execution of investigator and supplier contracts and amendments. Responsible for ensuring all contractual terms and conditions are based on the approved GSK Master template
• Accountable for negotiation and execution of other legal documents which may include, Confidential Disclosure Agreements, ICF compensation clause changes and Data Privacy clause changes. Develop and maintain accurate.
• Develop and maintain accurate tracking information related to site and supplier contracts, and external costs. Responsible for collaborating with legal counsel and procurement to maintain Clinical Operations Master.

Amersfoort, Utrecht, Nederland

• Activities/responsibilities:
• Providing support in the initial contract negotiations of CTAs in Belgium and the Netherlands
• Leading the budget development, negotiation and execution of amendments of CTAs of clinical trials in Belgium and the Netherlands
• Ensuring that all contractual terms and conditions are based on approved GSK master templates and are compliant with GSK Policies and SOPs.
• Ensuring that the budgets meet fair market value and are consistent with the… Show more Activities/responsibilities:
• Ensuring that the budgets meet fair market value and are consistent with the protocol

Amersfoort, Utrecht, Nederland

• Activities/responsibilities
• Providing support in the initial contract negotiations of CTAs in Belgium and the Netherlands
• Leading the budget development, negotiation and execution of amendments of CTAs of clinical trials in Belgium and the Netherlands
• Ensuring that all contractual terms and conditions are based on approved GSK master templates and are compliant with GSK Policies and SOPs.
• Ensuring that the budgets meet fair market value and are consistent with the… Show more Activities/responsibilities
• Ensuring that the budgets meet fair market value and are consistent with the protocol

Zeist

• Activities/responsibilities
• Acting as LOC EFPIA disclosure Champion, within GSK Pharma, GSK Consumer and ViiV HC. Point of contact for these entities when it comes to determining whether or not an -indirect- transfer of value to a healthcare.
• Ensure a complete and accurate reporting of all Transfer of Values in the SAP/CERPS EFPIA Operating module and publish… Show more Activities/responsibilities
• Ensure a complete and accurate reporting of all Transfer of Values in the SAP/CERPS EFPIA Operating module and publish financial relationships with HCPs, HCOs and patient organizations in the Transparency Registers of.
• Acting in accordance with the requirements of the CGR (NL), Sunshine Act (BE), APL Code (LUX) and GSK Global guidelines in order to guarantee high quality of the data to be published.
• Thinking along, identifying and suggesting possible points for improvement in the end-to-end (preparation of contracting up to disclosure of financial relationship) process

Zeist

• Activities/responsibilities
• Acting as LOC EFPIA disclosure Champion, within GSK Pharma, GSK Consumer and ViiV HC. Point of contact for these entities when it comes to determining whether an -indirect- transfer of value to a healthcare.
• Ensure a complete and accurate reporting of all Transfer of Values in the SAP/CERPS EFPIA Operating module and publish financial… Show more Activities/responsibilities
• Ensure a complete and accurate reporting of all Transfer of Values in the SAP/CERPS EFPIA Operating module and publish financial relationships with HCPs, HCOs and patient organizations in the Transparency Register of.
• Acting in accordance with the requirements of the CGR (NL) and GSK Global guidelines in order to guarantee high quality of the data to be published.
• Thinking along, identifying, and suggesting possible points for improvement in the end-to-end (preparation of contracting up to disclosure of financial relationship) process

Zeist

Opstellen van contracten en voortgang monitoren. Registreren van vendors, in opdracht aanmaken van inkooporders in SAP ERP. Ondersteunen interne klant bij gebruik van SAP ERP (rol van Super User).Ondersteuning verlenen bij het organiseren van bijeenkomsten.Coördineren van multichannel werkzaamheden (o.a. mailingen en drukwerk).Documentbeheer: verzamelen.

Zeist

Ondersteuning totstandkoming vergoedingsdossiers (editing/layout, database met literatuur vullen, koppelen van referenties in dossierstukken, afstemming met drukker).Detailplanning opstellen/onderhouden van alle activiteiten/deliverables behorende bij een vergoedingsaanvraag van een product (wie, levert wat, wanneer) en alle betrokkenen aanspreken/najagen.

Zeist

Zelfstandig beheren van systemen en documenten die gebruikt worden om de voortgang van studies te monitoren of bedoeld zijn om gegevens die van belang zijn voor de studie vast te leggen. Klaarmaken van de Investigator en Sponsor Files ten behoeve van de initiatie van deelnemende centra aan klinische studies. Het in opdracht van het studieteam zorgdragen.

Zeist

Ondersteunen en begeleiden van onderzoekscentra voor het toegankelijk maken en invullen van het electronisch studieboek (eCRF).Mede ontwikkelen van een datavalidatie systeem voor het ontsluiten van de electronisch verzamelde klinische onderzoeksdata en validatie van de betreffende data.Opzetten van data management plan ten einde juiste studie data analyse.

Hilversum

Coördineren van onderhoud/aanpassingen aan websites.Inplannen/instrueren van medewerkers (designer, programmeur, redacteur).Contact met klant (juiste wensen in kaart brengen + terugkoppeling).Facturering

Zeist

Opzetten van data management plan ten einde juiste studie data analyse te kunnen maken.Ontwerp, maken of helpen bij het opzetten van de database van klinisch onderzoek in het klinische data management systeem.Checks programmeren voor het datavalidatie proces (opsporen onvolledige, inconsistente of niet-aannemelijke data).Het opzetten en onderhouden van.

Zeist

Kwaliteitsbewaking van de opbouw van het salarisverloop.Kwaliteitsbewaking van de gegevens voor parttime percentages, het WAO dienstverband en de vrijstelling voor pensioen premie. Aanpassen van de pensioengegevens in diverse databestanden.

Amsterdam

Beheer van de voorraad.Contact met leveranciers.Debiteuren/crediteuren administratie. Kwaliteitsbewaking van orders van klanten.

Zeist

Controle van de 24-uurs registratie van de hartfunctie van patiënten

Hollansche Rading

Beheer van apotheek gedurende parate dienstperiode

Chemie/Scheikunde (Chemistry)

Diploma behaald, juni 1992

Education record

Diploma behaald, juni 1988