Search suggestions:

jovem aprendiz
home office
sem experiência
rh
auxiliar produção
recepcionista
engenheiro civil
técnico enfermagem
freelancer final de semana
auxiliar administrativo
caixa
almoxarife
motorista
Região Metropolitana de Belo Horizonte
São Paulo
Paraná
Minas Gerais
Região Metropolitana de Campinas
Região Metropolitana de São Paulo
Região Metropolitana de São José do Rio Preto
Rio Grande do Norte
Alagoas
Rio de Janeiro
Santa Catarina
Região Integrada de Desenvolvimento do Distrito Federal e Entorno
Apply

Clinical Research Associate II

MSD
Full time
há 2 dias

Job Description

Join Our Team as a Clinical Research Associate II!


Are you an experienced clinical research professional ready to take the next step in your career? We are seeking a Clinical Research Associate II to join our team. In this advanced role, you will develop strong site relationships and be responsible for effective site management throughout all phases of clinical research trials.


Key Responsibilities:

Main Requirements:

Are you ready to advance your career and play a crucial role in enhancing clinical research? Apply now and become a vital part of our mission to improve healthcare!

ClinicalTrialsBR

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

75%

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Required Skills:

Clinical Research, Clinical Research Trials, Clinical Studies, Clinical Trial Management, Clinical Trial Management Systems (CTMS), Clinical Trials, Communication, CO Monitoring, Electronic Trial Master File, Following Protocols, Good Clinical Practice (GCP), ICH GCP Guidelines, On Site Monitoring, Procedural Documentation, Regulatory Documents, Site Management, Standard Operating Procedure (SOP), Study Start Up, Trial Master Files

 Preferred Skills:

Job Posting End Date:

07/6/2025

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Save Apply
Report job
Other Job Recommendations:

Study Start-Up Clinical Research Associate (SSU CRA)

Novartis
São Paulo, São Paulo
R$ 30.942 - R$ 39.179
  • Supports country SSU strategy in close collaboration with...
  • Collaborates with SSO Study Start-Up Manager, SSO Study...
há 3 semanas

Clinical Research Associate II

Fortrea
Região Metropolitana de São Paulo, São Paulo
R$ 31.958 - R$ 40.466
  • Conducts site monitoring responsibilities for clinical...
  • Prepares and implements project plans related to Clinical...
há 3 semanas

Clinical Research Coordinator -Consultoria em Controle de Infecção Hospitalar _Belo Horizonte

IQVIA
São Paulo
  • Verifying and/or correcting research study information on...
  • Accurate input of trial data into the Electronic Data...
há 3 semanas

Clinical Research Coordinator - Rede Sao Camilo _Vila Mariana_ Sao Paulo_ Fix term_ Full time BRAZIL

IQVIA
São Paulo
  • Verifying and/or correcting research study information on...
  • Accurate input of trial data into the Electronic Data...
há 3 semanas

Clinical Research Coordinator -IDOR Salvador, Bahía (Part Time)

IQVIA
São Paulo
  • Verifying and/or correcting research study information on...
  • Accurate input of trial data into the Electronic Data...
há 3 semanas