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Clinical Research Associate
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Job Description
- Req#: JR000384
Employer Industry: Clinical Research
Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Supportive and collaborative work environment
- Chance to work on innovative clinical trials that contribute to healthcare advancements
- Competitive salary and benefits package
- Flexibility to manage monitoring activities independently
- Engage in a role that emphasizes quality and compliance in clinical research
What to Expect (Job Responsibilities):
- Conduct site monitoring responsibilities for clinical trials, ensuring compliance and quality
- Provide guidance and oversight to the CRA team to adhere to project scope and timelines
- Perform qualification, initiation, interim, and close-out visits both remotely and onsite
- Maintain regular contact with study sites to ensure protocol and GCP compliance
- Collaborate with cross-functional departments to resolve clinical trial monitoring issues
What is Required (Qualifications):
- Bachelor's Degree in a scientific health field
- Minimum of 2 years of on-site monitoring experience in clinical trials
- Proven ability to establish and maintain positive relationships with stakeholders
- Strong organizational skills and ability to manage multiple priorities effectively
- Excellent communication and interpersonal skills, with a customer service orientation
How to Stand Out (Preferred Qualifications):
- Experience in oncology monitoring
- Knowledge of clinical research regulations and ethical requirements
- Familiarity with clinical trial management systems and electronic data capture
- Ability to problem-solve unstructured or ambiguous challenges
- Proficiency in local language, both written and verbal, where monitoring occurs
#ClinicalResearch #CRA #CareerOpportunity #ClinicalTrials #HealthcareInnovation
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