Clinical Research Assistant

• Aqualane Clinical Research is a comprehensive clinical research group dedicated to advancing medical therapies across a broad range of human disease states. The organization offers patients the opportunity to participate in the development of treatments where none currently exist or where safer, more effective options are needed. By collaborating closely with patients, their care partners, and industry sponsors, Aqualane Clinical Research focuses on the safe and ethical evaluation of emerging therapies. The team is committed to rigorous scientific standards and patient-centered care throughout the research process.

Job Title:

Clinical Research Assistant

Job Description:

The Research Assistant at a clinical research site plays a vital role in supporting the activities of the research team, ensuring the smooth operation of clinical trials and studies conducted at the site. This position involves a combination of administrative, logistical, and research-related tasks aimed at facilitating the efficient conduct of clinical research activities.

Responsibilities:

1. Administrative Support:

◦ Assist with the organization and maintenance of study-related documentation, including participant records, and study protocols.

◦ Coordinate scheduling of participant visits and study procedures, ensuring adherence to protocol timelines and requirements.

◦ Maintain accurate and up-to-date study databases, electronic records, and tracking systems.

2. Participant Recruitment and Screening:

◦ Assist in the recruitment of study participants through outreach efforts, screening of potential participants, and obtaining informed consent.

◦ Ensure participant eligibility criteria are met and documented according to study protocols and regulatory requirements.

◦ Maintain confidentiality and privacy of participant information throughout the recruitment and screening process.

3. Study Procedures and Data Collection:

◦ Support the implementation of study procedures and data collection activities, including participant assessments, sample collection, and study interventions.

◦ Assist with the collection, recording, and management of study data, ensuring accuracy, completeness, and compliance with protocol requirements.

◦ Collaborate with the research team to resolve data discrepancies and implement corrective actions as needed.

4. Logistical Support:

◦ Provide logistical support for study-related activities, including ordering and maintaining study supplies, coordinating shipments, and managing study equipment.

◦ Assist with the coordination of study visits, participant transportation, and other logistical arrangements as needed.

◦ Collaborate with external vendors, sponsors, and stakeholders to facilitate study-related logistics and operations.

Qualifications:

• Bachelor's degree in life sciences, healthcare, or a related field.

• Previous experience in clinical research, healthcare, or a related field preferred but not required.

• Strong organizational, communication, and interpersonal skills.

• Detail-oriented with the ability to multitask and prioritize responsibilities effectively.

• Proficiency in Microsoft Office applications and electronic data management systems.

• Knowledge of regulatory requirements and guidelines governing clinical research (e.g., GCP, ICH) is advantageous.

Please email resumes to: Brittany@AqualaneResearch.com