Jobs · Analyst · Maryland

Clinical Research Coordinator I - Bilingual (Spanish)

ObjectiveHealth · Laurel, MD · 1 mo ago
AnalystFull-time

About the role

ObjectiveHealth is a clinical research company dedicated to improving patient outcomes through the use of proprietary technology. Our services include increasing patient access to research trials, enhancing physician care options, and delivering superior clinical research enrollment metrics to pharmaceutical sponsors.

Responsibilities

- Conducting IRB-approved clinical trial protocols including patient identification, screening, randomization, and enrollment. - Performing and assisting with direct patient care activities such as consenting patients, physical assessments, blood draws, medication administration, ECGs, and reporting adverse events and serious adverse events. - Maintaining accurate and compliant data entry, ensuring regulatory compliance, and adhering strictly to study protocols. - Communicating effectively with leadership, coworkers, and stakeholders, including physicians, sponsors, monitors, and other relevant parties. - Staying focused and organized while managing multiple protocols, responding to IRB requests, and maintaining eSource materials for assigned studies. - Demonstrating a strong commitment to the company's values and initiatives, fostering positive relationships, and embodying a dedication to innovation and excellence.

Requirements

- Certification in areas such as MA, phlebotomy, or equivalent. - Strong interpersonal skills and a bias for action. - Proficiency in all aspects of conducting clinical trials, including patient interactions, consent processes, physical assessments, and medical procedures. - Excellent attention to detail and the ability to maintain clean, compliant data entries. - Effective communication skills and the ability to build and maintain relationships with various stakeholders. - Ability to remain focused and manage multiple tasks simultaneously. - Legal authorization to work in the United States.

Qualifications

- Experience in patient care and clinical research. - Strong organizational and attention to detail skills. - Excellent communication and interpersonal skills. - Ability to work independently and as part of a team. - Familiarity with regulatory requirements and compliance standards.

Skills

- Strong interpersonal and communication skills. - Ability to handle multiple tasks and protocols efficiently. - Attention to detail and accuracy in data entry. - Organizational skills and the ability to prioritize tasks. - Knowledge of regulatory requirements and compliance standards.

Benefits

- Competitive compensation package. - 401(k) plan with company match. - Clear career progression opportunities. - Short- and long-term disability coverage. - Health savings and flexible spending accounts. - Comprehensive health, dental, and vision insurance plans. - Generous paid time off and vacation days. - Adoption assistance, paid holidays, and a variety of voluntary benefits.

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