Oferty pracy: clinical research associate
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- Icon plcWarszawa, mazowieckiePostedOpublikowano 16 dni temu·
- Work with functional management, Business Development (BD) and clinical study teams, proactively and when requested, to ensure resource requests are resolved…
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- Everest Clinical ResearchWarszawa, mazowieckiePostedOpublikowano ponad 30 dni temu·
- At least two years' drug safety experience in a pharmaceutical or clinical research environment.
- Perform reconciliation of safety data between clinical and…
- Zobacz wszystkie oferty pracy praca: Everest Clinical Research – Warszawa – praca: Clinical Associate - Warszawa, mazowieckie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Clinical Trial Drug Safety Associate"
- PfizerHybrydowo in Warszawa, mazowieckiePostedOpublikowano 13 dni temu·
- Operational experience in clinical trial management or healthcare industry (pharmaceuticals, life sciences, and medical).
- Zobacz wszystkie oferty pracy praca: Pfizer – Warszawa – praca: Operations Associate - Warszawa, mazowieckie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Medical Operations Associate", lokalizacja: Warszawa, mazowieckie
Wyświetl podobne oferty pracy tego pracodawcyParexelzdalniePostedOpublikowano ponad 30 dni temu·- Good understanding and working knowledge of clinical research, clinical trial phases, current GCP/ICH and country clinical research legislation and guidelines.
- Zobacz wszystkie oferty pracy praca: Parexel – zdalnie – praca: Clinical Research Associate - zdalnie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Senior Clinical Research Associate - FSP (Kraków/Katowice/Silesia))", lokalizacja: zdalnie
- PfizerHybrydowo in Warszawa, mazowieckiePostedOpublikowano 13 dni temu·
- Experience in the pharmaceutical industry, clinical research, or healthcare related field.
- Individual filling the position are responsible for the project…
- Zobacz wszystkie oferty pracy praca: Pfizer – Warszawa – praca: Associate Manager - Warszawa, mazowieckie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Associate - Aggregate Report Coordinator", lokalizacja: Warszawa, mazowieckie
- KCRZdalniePostedOpublikowano ponad 30 dni temu·
- Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines;
- Zobacz wszystkie oferty pracy praca: KCR – zdalnie – praca: Clinical Research Associate - zdalnie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Clinical Research Associate II/Senior Clinical Research Associate", lokalizacja: zdalnie
- Thermo Fisher ScientificHybrydowoPostedOpublikowano 13 dni temu·
- Basic understanding of clinical supply operations.
- Good understanding of clinical supply operations, including facility maintenance and certification,…
- Zobacz wszystkie oferty pracy praca: Thermo Fisher Scientific – zdalnie – praca: Trading Manager - zdalnie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Associate Trade Compliance Manager - Global Clinical Supplies", lokalizacja: zdalnie
- PSI CROWarszawa, mazowieckieZwykle odpowiada w ciągu 2 dniPostedOpublikowano ponad 30 dni temu·
- Communication point for investigative sites participating in the clinical research projects.
- Join our international team and be the key support to clinical…
- Zobacz wszystkie oferty pracy praca: PSI CRO – Warszawa – praca: Management Associate - Warszawa, mazowieckie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Site Management Associate"
- ICONzdalniePostedOpublikowano ponad 30 dni temu·
- Populate trial details in national clinical trial registries (e.g., NMRR, HSA.
- Support COM/CTL in Trial Portfolio Discussion/Review.
- Zobacz wszystkie oferty pracy praca: ICON – zdalnie – praca: Senior Associate Engineer - zdalnie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Senior Study Start Up Associate"
- IQVIAzdalnieZwykle odpowiada w ciągu 7 dniPostedOpublikowano ponad 30 dni temu·
- Strong experience in monitoring of clinical trials.
- Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and…
- Zobacz wszystkie oferty pracy praca: IQVIA – zdalnie – praca: Clinical Research Associate - zdalnie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Senior Clinical Research Associate, Sponsor dedicated in POLAND", lokalizacja: zdalnie
- Thermo Fisher Scientific40-040 KatowicePostedOpublikowano ponad 30 dni temu·
- Alongside clinical research through our PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient…
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- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Associate Outreach Coordinator"
Wyświetl podobne oferty pracy tego pracodawcyMedpace, Inc.Hybrydowo in 02-092 WarszawaPostedOpublikowano ponad 30 dni temu·- Medpace is a full-service clinical contract research organization (CRO).
- Compile and maintain project-specific status reports within the clinical trial…
- Zobacz wszystkie oferty pracy praca: Medpace, Inc. – Warszawa – praca: Clinical Trial Administrator - Warszawa, mazowieckie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Associate Clinical Trial Manager (PhD) - Radiopharmaceuticals"
- Thermo Fisher Scientific81-537 GdyniaPostedOpublikowano 22 dni temu·
- Alongside clinical research through our PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient…
- Zobacz wszystkie oferty pracy praca: Thermo Fisher Scientific – Gdynia – praca: Associate Manager - Gdynia, pomorskie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Associate Manager Sites"
- Innovaderm ResearchzdalniePostedOpublikowano 2 dni temu·
- At least 8 years of experience in clinical regulatory affairs in the pharmaceutical, biotechnology and/or CRO industry.
- Liaise with cross-functional leads.
- Zobacz wszystkie oferty pracy praca: Innovaderm Research – zdalnie – praca: Director of Regulatory Affairs - zdalnie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Associate Director, Regulatory Affairs (Poland)"
- Icon plcWarszawa, mazowieckiePostedOpublikowano 9 dni temu·
- Previous experience in clinical research or regulatory affairs preferred, but Nt required.
- Assisting in the preparation and submission of regulatory documents,…
- Zobacz wszystkie oferty pracy praca: Icon plc – Warszawa – praca: Associate - Warszawa, mazowieckie
- Przeglądaj wynagrodzenia: wynagrodzenia na stanowisku "Study Start Up Associate - submissions", lokalizacja: Warszawa, mazowieckie
Job Post Details
PRM Associate II - job post
3.43.4 na 5 gwiazdek
Warszawa, mazowieckie
Pełny etat
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Opis stanowiska
Oto, co w opisie oferty pracy pokrywa się z Twoim profilem.Wymiar pracy
- Pełny etat
Lokalizacja
Warszawa, mazowieckie
Pełny opis stanowiska
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
To be successful in the role, you will have:
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Propose staff and provide CVs for potential projects, following agreement of applicable functional counterparts e.g. CRA Managers or CTM Directors, focusing on the skill sets required by the Sponsor and the availability during the timeframe of the study
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Oversee and update the resource management database tool in relation to staff allocation to projects, as appropriate and issue allocation reports etc as required
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Maintain and improve accuracy of information stored in the resourcing database for the assigned staff pool re reservations, unfilled requirements, skills and all other PRM-maintained information. Ensure updates are submitted to the designated PRM colleagues in a timely manner and contain accurate information; Provide regular and ad hoc reports and information to functional leadership which is up to date, accurate and timely. Support CV database management
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Support PRM Manager in providing clear and detailed information for inclusion in proposals after reviewing RFIs and RFP
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Produce and analyse reports that accurately forecast future resource needs/resource availabilities, required skills, headcount to sell, and recovery and utilisation rates
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Ensure optimisation of assigned versus costed resources by carrying out a continuous review of resource allocation to projects and highlighting discrepancies
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Work with functional management, Business Development (BD) and clinical study teams, proactively and when requested, to ensure resource requests are resolved within the Service Level Agreement (SLA) timelines; communicate with all parties in a timely manner, to support customer satisfaction
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Solve problems where technical expertise and knowledge of precedents enables identification of possible solutions and underpins making of judgement
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Undertake other reasonably related duties as may be assigned from time to time
To be successful in the role, you will have:
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Graduate level education
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Strong communication skills
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Highly organised
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Experience of working in a reporting role
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Advanced Excel skills is essential
Benefits of working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
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Various annual leave entitlements
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A range of health insurance offerings to suit you and your family’s needs.
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Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
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Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
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Life assurance
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Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
Visit our
careers site
to read more about the benefits ICON offers.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request
here
.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
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