•Clinical Research Coordinator needed in Hollywood, FL (Spanish-Speaker)
HealthPlus StaffingHollywood, FL, USjob_description.job_card.variable_hours_ago
serp_jobs.job_preview.job_type
- serp_jobs.job_card.full_time
job_description.job_card.job_descriptionHealthcare related background, such as FMD (Foreign Medical Doctor) NP, LPN, or RN. At least two years of experience as a Clinical Research Coordinator. Proficient in Spanish. Excellent communication, organizational, and problem-solving skills. Ability to prioritize tasks effectively. Ability to work independently and as part of a team. Ability to work in a fast-paced environment. Knowledge of applicable federal and state regulations. Knowledge of clinical research processes and procedures. Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, etc.).
Job Description
Job Description
Medical Research Coordinator (Full Time) - Hollywood, FL (Spanish-speaker)
We are looking for an experienced, bilingual (Spanish-speaking) Medical Research Coordinator to join our research team in Hollywood, FL. The Medical Research Coordinator will be responsible for the coordination of clinical research studies while ensuring compliance with all applicable regulations and guidelines. The ideal candidate will possess a strong understanding of clinical research, clinical trials, and the medical field. The Medical Research Coordinator should have excellent communication, organizational, and problem-solving skills with an ability to prioritize tasks effectively.
Responsibilities
- Develop and maintain clinical study documents and coordinate all aspects of clinical trials including case report forms, informed consents, and other regulatory documents.
- Monitor clinical trials and ensure that they are conducted in accordance with protocols, standard operating procedures, and applicable regulations.
- Train, support and delegate tasks to clinical research staff.
- Conduct data review and analysis.
- Develop and manage budgets, timelines, and communications.
- Ensure compliance with all applicable federal, state, and local regulations.
- Maintain accurate records of research activities and submit reports to the appropriate authorities.
- Develop and implement strategies for data collection.
- Work with study investigators to ensure that the study is conducted in compliance with the protocol.
- Develop study-related materials and provide support to investigators.
- Provide guidance to investigators on the interpretation and implementation of the protocol.
- Coordinate and participate in monitoring visits.
- Perform other duties as assigned.
Requirements
If you are an experienced Medical Research Coordinator who is looking for a new opportunity in Hollywood, FL, we encourage you to apply today!
The HealthPlus Team
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Clinical Research Coordinator • Hollywood, FL, US
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