Werken bij Heraklespharma


Soort organisatie
Werving & selectie / uitzendbureau
Aantal medewerkers
Internationaal actief

Plan route



(Sr.) Clinical Research Associate / CRA EXCLUSIEF (homebased)
We are currently seeking experienced indivduals to join our client, a growing global CRO, in the position of (Senior) CRA / Clinical Research Associate. Positions are nationwide and are regional home based with the highest level of flexibility! Our client directly offers a permanent contract!  Responsibilities: Perform feasibility studies (pre-study site selection) when required; Conduct all level of monitoring visits in accordance to GCPs and applicable local and international regulations and SOPs. This encompasses clinical trial material (CTM) accountability, regulatory document review and submission (as appropriate), clear andcomplete trip report writing and site management; Provide mentoring and coaching to colleagues and site staff when needed; Manage/advise teams in therapeutic areas of proficiency as required or appropriate; Design monitoring tools as requested; Provide support for the design of CRFs and protocols as requested; Develop monitoring plans when required; Actively participate in study team meetings; Actively participate in investigator meetings; Conduct training for colleagues or study team as requested; Manage a cost center and implement appropriate actions to keep within budget.Interested in this position as a (Senior) CRA / Clinical Research Associate? Please contact Rob Helmich through the website. Our client has deliberately chosen to handle this recruitment & selection proces by Herakles. For questions you can alsso call +31 6 538 538 92 / – e-mailadres niet toegestaan – 14 dagen geleden
Clinical Project Manager (doorgroei CRA mogelijk)
Central point of communication between the company and the Investigator for all clinical trial related activities to assure trials are conducted on time and budget, while fully GCP, ICH and Company SOP compliant. Leads internal teams to coordinate on the local CPO and/or the global level for a combined portfolio of large and smaller clinical trials in different complexity levels, when assigned. Participate in operational feasibility to assess feasibility of trial in Netherlands Nominate new sites for clinical trials; analyze capability and make recommenda-tion for trial inclusion. Assume ambassadorial role to facilitate communication between sites and company line functions and increase value proposition to investigators. Facilitate preparation and collection of site level documents; resolve problems as   required. Perform site selection visits. Create and oversee entire site management, including initiation and training, monitoring and close-out visits, regulatory assessment, drug supply management and resolution of site problems to ensure compliance.  Track trial execution milestones; monitor trial costs; identify problems; resolve is-sues and escalate as appropriate. Manage recruitment and execute contingency plans, as needed. Assure preparation/generation of study monitoring reports. Conduct site contract negotiations.   Manage data at the site; resolve technical and content issues to achieve aggressive database lock targets. Act as local and/or global “Lead CRA” and author global monitoring plan. Act as a mentor to new associates, as assigned. Participate in multi-disciplinary teams within CPO and globally to evaluate and implement process improvement.Interesse in deze positie? Onze opdrachtgever heeft er bewust voor gekozen om de vacature en werving & selectieprocedure door Herakles te laten behandelen. Neem hiervoor contact op met Albert Hollemans +31 6 22639519 / – Klik op de solliciteer-button om te solliciteren – (avonduren geen probleem).  27 dagen geleden
Experienced Clinical Team Manager
This exciting and unique role could take you to the next step of your career within Clinical Research. The role coordinates all aspects of clinical activities on an international basis. This includes the day to day management and leadership of a team of Clinical Research Associates who are allocated to a project on a Country basis. You will work in partnership with the Project Manager to ensure the necessary training, tracking and quality systems are in place for the clinical team, and be primarily responsible for the clinical deliverables of the Project within agreed timelines and budget. Clinical Team Managers/ Clinical trials provide contact and support to the project sponsor for all clinical aspects. We are seeking high performing individuals who enjoy a fast-paced environment and have had Clinical Project Management experience and exposure to international studies, involving the coordination of CRAs across different countries. With your excellent written and oral English skills you will have exceptional interpersonal and problem solving skills, with the ability to lead CRAs in different countries. You will also have proficient working knowledge of GCP and experience in several medical / therapeutic areas. You must be comfortable working in a matrix management system and have the ability to motivate, mentor and integrate international teams. Sounds like you? We are seeking highly motivated and skilled applicants who will want to share in our continued growth in the international market place. If you succeed we can offer you the opportunity to grow into enhanced roles within the department and also have examples of Clinical Team Managers who have moved into project management or management of CRAs. We will consider field based applicants depending on your experience level.Interested in this position as experienced Clinical Team Manager/ Clinical Trials? Contact Albert Hollemans via – e-mailadres niet toegestaan – / +31 6 22639519 (evening hours are no problem) 30+ dagen geleden
Cathlab Nurse
Wij zijn op zoek naar een enthousiaste, zelfstandige en accuraat handelende cardiovasculair laborant in opleiding die specifieke, stressrijke omstandigheden niet uit de weg gaat. Ben je al cardiovasculair laborant (HCK medewerker) en ervaring opgedaan in een hartkatheterisatiecentrum of interventiecentrum dan gaan wij ook graag met je in gesprek. De afdeling waarop je komt te werken is dynamisch, goed geoutilleerd en biedt, door constante en continue innovaties, jou alle kans om je blijvend te ontwikkelen binnen een professionele groep collega’s. Ook is het een acuut infarctcentrum met een regionale functie. Je assisteert arts-assistenten en interventiecardiologen bij het uitvoeren van o.a. hartcatheterisaties, dotterprocedures, drukmetingen en diverse klepimplantaties. Gedurende de opleiding heb je regelmatige dagdiensten. Na het afsluiten van de inwerkperiode ga je starten met bereikbaarheidsdiensten. Totale duur van de opleiding is ongeveer twee jaar bestaat uit de volgende onderdelen: theoretische CCU-opleiding praktijkopleiding binnen de afdelingRöntgen Cardiologie opleiding stralingshygiëne 5 A (alleen voor verpleegkundigen)Voor meer en specifieke informatie over deze functie kun je contact opnemen Tom van der Poel +31 651846575 30+ dagen geleden
Clinical Research Associate
For an international study, our client is looking for ambitious experienced Dutch speaking CRA's. Next to organizing and monitoring an international clinical trial in The Netherlands, you will ensure the quality of clinical data. You will work in the headquarters in Utrecht from where the international study is globally managed. You will work in the global project team. Ideas are shared by the global project team in the Netherlands. You are encouraged to share your ideas about improvements in the study and share these ideas also with the global project team. TASKS AND RESPONSIBILITIES Involved in the start -up of the study and carry out pre-study visits; Monitors clinical research in acccordance with the protocol, sops, applicable laws and ich/gcp guidelines, including visit report compilation and follow-up within the set timelines; Collates and verifies the case report form (crf's) for completeness and accuracy by verifying the source documents, e.g. medical file, laboratory results; Ensures the correct query process is followed in collaboration with the data management team; Ensures the correct reporting and follow-up of adverse events, serious adverse events and suspected unexpected serious adverse reactions; Verifies compliance with procedures relating to drug accountability; Develops and maintains an effective working relationship with site staff; Trains investigators and site staff (including laboratory, pharmacy and other staff involved) in the correct implementation of the protocol, the crf and study-specific procedures; Supports the investigator during inspections by healthcare authorities or audits; Ensures the reliable documentation and archiving of study documents, both at the investigator and "in-house"; Partipates in and helps to organize meetings for investigators and cra's; Ensures that information is conveyed effectively between the sponsor, investigator and project team; Collaborates closely with internal and external contacts; Is involved in sop development, maintenance and training. Interested in this position? Please contact Albert Hollemans through the website. For questions you can also call 06 - 22639519 30+ dagen geleden
Clinical Compliance Manager
Werken binnen Compliance betekent dat elke dag anders is! De ene dag ontwikkel je procedures, de andere dag creëer je een tool of trainingsprogramma voor CRA's. Of je werkt aan een workshop voor Project Managers, organiseert Investigator meetings, reist naar het buitenland om CRA's te trainen en te coachen. Een ding is zeker: je bent voortdurend in contact met mensen binnen en buiten de organisatie. Onze opdrachtgever zoekt voor hun Training en Compliance afdeling een enthousiaste en professionele nieuwe collega. Je gaat werken in een team samen met 5 collega's. Het is een dynamisch team van professionals die allemaal hebben gewerkt als (Senior) CRA en/of Lead CRA.Interesse in deze positie? Mail of bel naar Rob Helmich – e-mailadres niet toegestaan – of +31 6 538 538 92 30+ dagen geleden


feed (heraklespharma)

Mogelijk interessante vacatures

Ervaren Fiscaal medewerker 24 uur
Amsterdam   Rousch
30+ dagen geleden
Assistent Accountant 2e stap!
Etten-leur   Rousch
7 dagen geleden
Gevorderd Assistent Accountant - Controlepraktijk
Zaandam   Rousch
7 dagen geleden
Senior Belastingadviseur (NOB)
Woerden   Rousch
30+ dagen geleden
Gevorderd Assistent Accountant
3 dagen geleden