Clinical Trial Coordinator

1 semana atrás


São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

Provides administrative and technical support to the Project Team. Supports audit readiness by ensuring files are reviewed according to the

schedule detailed in the organization's SOP and department guidance document. Provides administrative support for site activation activities.

Aids the development of the critical path for site activation within assigned projects in support of rapid site activations. Represents CRG

personnel. May utilize local knowledge, organization systems, external site lists and sponsor directives to develop and review site lists that

are suitable for the strategic needs of feasibility activities and to provide local input into the site tiering process. May act as a buddy during

onboarding phase and provide training to new staff as needed.

Qualifications:Education and Experience: High / Secondary school diploma or equivalent and relevant formal academic / vocational

qualification. Bachelor's degree preferred. Previous experience that provides the knowledge, skills, and abilities to perform the job

(comparable to 0 to 1 year). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly

related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities: Ability to work in a team or independently as required Good organizational skills and strong attention to

detail, with proven ability to handle multiple tasks efficiently and effectively Demonstrated ability to effectively analyze project-specific

data/systems to ensure accuracy and efficiency Strong customer focus Flexibility to reprioritize workload to meet changing project

timelines Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical

Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout

Good English language and grammar skills and proficient local language skills as needed Good computer skills, proficient in MS Office

(Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems Ability to successfully

complete the organizations clinical training program Self-motivated, positive attitude and good interpersonal skills Effective oral and

written communication skills Good interpersonal skills Essential judgment and decision-making skills Capable of accurately following project work instructions Good negotiation skills Independent thinker Ability to manage risk and perform risk escalation appropriately


  • Clinical Project Manager

    1 semana atrás


    São Paulo, São Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro

    Clinical Project Manager(Level Depends on Experience)Job Purpose/Summary: Responsible for management and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client's goals of time, budget and quality performance are met. The Clinical Project Manager I is expected to require support and guidance from Directors and/or advanced Clinical...

  • Clinical Trial Educator

    1 semana atrás


    São Paulo, São Paulo, Brasil Novasyte Tempo inteiro

    Job OverviewThe Clinical Trial Educator (CTE) will provide information and education on clinical trial inclusion and exclusion criteria to trial coordinators and healthcare providers. Also provides in-service presentations with the goal to increase patient enrollment. Works in partnership with CRAs and other field-based medical teams for optimal trial...


  • São Paulo, São Paulo, Brasil Iqvia Argentina Tempo inteiro

    Are you looking for an opportunity in Clinical Research?Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us IQVIA are looking Clinical Research Coordinator. This role has an immediate start working 40 hours a week for a period...


  • São Paulo, São Paulo, Brasil Iqvia Argentina Tempo inteiro

    Are you looking for an opportunity in Clinical Research?Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us IQVIA are looking Clinical Research Coordinator. This role has an immediate start working 40 hours a week for a period...


  • São Paulo, São Paulo, Brasil Iqvia Argentina Tempo inteiro

    Are you looking for an opportunity in Clinical Research?Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us IQVIA are looking Clinical Research Coordinator. This role has an immediate start working 24 hours a week for a period...

  • Clinical Trial Manager

    1 semana atrás


    São Paulo, São Paulo, Brasil Iqvia Llc Tempo inteiro

    (Senior) Clinical Trial Manager - Sponsor Dedicated page is loaded (Senior) Clinical Trial Manager - Sponsor Dedicated Apply locations São Paulo, Brazil Mexico City, Mexico Santiago, Chile Buenos Aires, Argentina Lima, Peru time type Full time posted on Posted 2 Days Ago job requisition id R Clinical Trial Manager – Sponsor Dedicated. Clinical Trial...

  • Clinical Trial Manager

    1 semana atrás


    São Paulo, São Paulo, Brasil Iqvia Argentina Tempo inteiro

    Clinical Trial Manager – Sponsor Dedicated. Clinical Trial Manager provides for the regional/global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure regional/global clinical operations deliverables progress according to agree upon timelines...

  • Clinical Trial Coordinator

    1 semana atrás


    São Paulo, São Paulo, Brasil Thermo Fisher Scientific Inc. Tempo inteiro

    Job Description Provides administrative and technical support to the Project Team. Supports audit readiness by ensuring files are reviewed according to the schedule detailed in the organization's SOP and department guidance document. Provides administrative support for site activation activities. Aids the development of the critical path for site activation...

  • Clinical Trial Manager

    1 semana atrás


    São Paulo, São Paulo, Brasil Novasyte Tempo inteiro

    Clinical Trial Manager - Sponsor Dedicated.Trial Management services provide local management of a clinical trial (s) (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned project(s) at the country level for end-to-end project management from start-up through to closeout...


  • São Paulo, São Paulo, Brasil Johnson & Johnson Tempo inteiro

    Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest...


  • São Paulo, São Paulo, Brasil Johnson And Johnson Tempo inteiro

    At Johnson & Johnson,we believe health is everything.Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the...


  • São Paulo, São Paulo, Brasil Johnson & Johnson Tempo inteiro

    Job Description - Contract Clinical Trial Senior Analyst W) Contract Clinical Trial Senior Analyst W Description At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are...

  • Clinical Trials Assistant 1

    1 semana atrás


    São Paulo, São Paulo, Brasil IQVIA Tempo inteiro

    Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...


  • São Paulo, São Paulo, Brasil CDS Fortrea Inc. Tempo inteiro

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Clinical Trial Manager

    1 semana atrás


    São Paulo, São Paulo, Brasil ICON plc Tempo inteiro

    Job Advert PostingICON 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...


  • São Paulo, São Paulo, Brasil Johnson & Johnson Tempo inteiro

    Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest...


  • São Paulo, São Paulo, Brasil Iqvia Tempo inteiro

    Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. Assist the clinical team with the preparation, handling, distribution, filing, and...


  • São Paulo, São Paulo, Brasil Parexel Tempo inteiro

    Working from home with occasional days in our office location in Sao Paulo, as an Initiation Clinical Research Associate (ICRA) you will be the direct point of contact with assigned sites located throughout South America and accountable for quality and delivery during the start-up phase. Duties will include EC submissions / site activation related...

  • Clinical Trial Assistant

    1 semana atrás


    São Paulo, São Paulo, Brasil Medpace, Inc. Tempo inteiro

    Job Summary:Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage...


  • São Paulo, São Paulo, Brasil MSD Tempo inteiro

    Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.Main responsibilities: With the support of the CRA Manager, acts as primary...