CRA 1 - Brazil job opportunity at IQVIA Holdings, Inc..

Home Jobs In Brazil Tag: Job CRA 1 - Brazil position at IQVIA Holdings, Inc.


bot
IQVIA Holdings, Inc. CRA 1 - Brazil
Experience: General
Pattern: full-time
Country:
apply Apply Now
Salary:
Status:

Job

Copy Link Report
degreeMaster's (M.A.)
loacation São Paulo, Brazil, Brazil
loacation São Paulo, Bra..........Brazil

Location:   Brazil (Sao Paulo) About Us:   Join our team and help shape the future of our organization. We are a leading company committed to excellence and innovation, seeking a talented Senior Recruiter to support our growth. Job Overview:  Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Key Responsibilities: Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. Basic Qualifications: Bachelor's Degree Degree in scientific discipline or health care preferred. Excellent command of English (written/spoken). Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Good therapeutic and protocol knowledge as provided in company training. Others requirements: Strong attention to detail and excellent communication skills. Exceptional problem-solving, judgment, and decision-making abilities. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Written and verbal communication skills including good command of English language. Organizational and problem-solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. Why Join Us? Be part of an innovative and forward-thinking company that collaborates to make a healthier world. Work alongside a diverse and talented team. Many opportunities for professional growth by developing project mgmt abilities. Competitive salary and benefits package. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

Other Ai Matches

Product Owner, HCP Data Applicants are expected to have a solid experience in handling HCP Data related tasks
Senior Data Team Lead, FSP Applicants are expected to have a solid experience in handling FSP related tasks
Associate/Director of Biostatistics, Rare Disease, FSP Applicants are expected to have a solid experience in handling Rare Disease, FSP related tasks
Study Delivery and Country Relations Manager - Oncology Evidence Network - Spain Applicants are expected to have a solid experience in handling Job related tasks
Clinical Trial Educator 1 Applicants are expected to have a solid experience in handling Job related tasks
Freelance- Translators/Linguists, Zulu into English Applicants are expected to have a solid experience in handling Zulu into English related tasks
Consultant, Strategy Consulting Applicants are expected to have a solid experience in handling Strategy Consulting related tasks
Junior Associate, Delivery Enablement Applicants are expected to have a solid experience in handling Delivery Enablement related tasks
Clinical Educator / Registered Nurse / RN - Novasyte Applicants are expected to have a solid experience in handling Job related tasks
MLT/Hematology Applicants are expected to have a solid experience in handling Job related tasks
Internal Medical Translator Japonais vers Anglais (Télétravail) / Internal Medical Translator Japanese to English (Remote) Applicants are expected to have a solid experience in handling Job related tasks
Pharmaceutical Sales Associate - Allentown, PA Applicants are expected to have a solid experience in handling PA related tasks
Product Owner, Health Data & Tokenization Applicants are expected to have a solid experience in handling Health Data & Tokenization related tasks
Attaché de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech Applicants are expected to have a solid experience in handling Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech related tasks
Cleveland, OH Clinical Educator - Registered Nurse Applicants are expected to have a solid experience in handling OH Clinical Educator - Registered Nurse related tasks
Sr Panel Admin Associate Applicants are expected to have a solid experience in handling Job related tasks
Site Contract Manager Applicants are expected to have a solid experience in handling Job related tasks
Inventory Control Assoc ll Applicants are expected to have a solid experience in handling Job related tasks
Enfermera Profesiona Homecare PSP Applicants are expected to have a solid experience in handling Job related tasks
Clinical Trial Educator: Autism and Hypertension Applicants are expected to have a solid experience in handling Job related tasks
Medisch Afgevaardigde Fythotherapie - Limburg Applicants are expected to have a solid experience in handling Job related tasks
Freelance- Translators/Linguists, English into Hungarian Applicants are expected to have a solid experience in handling English into Hungarian related tasks
MedTech Travel RN- Device Liaison Applicants are expected to have a solid experience in handling Job related tasks