About the Client: USA is a well-established organization providing innovative solutions and career opportunities. The company is based in [Clinical trial monitoring, Regulatory documentation, GCP compliance, Site initiation & closure, Patient safety & data collection, Protocol adherence, Clinical data review, Communication & reporting].We are seeking a highly motivated and skilled Sr. Clinical Research Associate to join our team at USA in [Clinical trial monitoring, Regulatory documentation, GCP compliance, Site initiation & closure, Patient safety & data collection, Protocol adherence, Clinical data review, Communication & reporting]. The ideal candidate will be responsible for delivering high-quality results, collaborating with cross-functional teams, and driving success in assigned projects.Key Responsibilities:- Perform day-to-day tasks related to Sr. Clinical Research Associate- Manage and optimize processes within the team- Design, develop, and implement solutions aligned with business needs- Collaborate with cross-functional teams and stakeholders- Ensure compliance with industry standards and best practicesRequired Skills & Qualifications:- Relevant technical and soft skills for the Sr. Clinical Research Associate role- Strong problem-solving and analytical abilities- Excellent communication and teamwork skills- Ability to adapt in a fast-paced environmentKeywords: Sr. Clinical Research Associate, USA, [Clinical trial monitoring, Regulatory documentation, GCP compliance, Site initiation & closure, Patient safety & data collection, Protocol adherence, Clinical data review, Communication & reporting]
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At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 1971.00/monthly.
