Clinical Research Coordinator II: Drive Impactful CNS Trials

CenExel; Marlton (NJ); On-site; USD 36,000 - 46,000; Full time

Benefits offered by this job

Health Insurance

Dental

Vision

Long-Term Disability

Short-Term Disability

Life Insurance

401k

Job summary

CenExel is seeking a Clinical Research Coordinator I to coordinate all aspects of clinical trials with strict adherence to ICH, GCP, and protocol guidelines. Located in Marlton, NJ, you will support study initiation through completion, collaborating with investigators, vendors, and sponsors to ensure data quality and participant safety.

The role requires strong communication, leadership, and problem-solving skills, with a focus on regulatory compliance, data integrity, and efficient study

Qualifications

• Must have proper experience and demonstrate mastery of Clinical Research Coordinator I position.
• High school graduate or equivalent; Bachelors Degree, preferred
• CCRC certification preferred
• 2-3 years of experience in the medical field, preferred
• Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
• Strong leadership and mentorship skills.
• Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
• Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations.
• Works independently as well as functioning as part of a team.
• Must be able to effectively communicate verbally and in writing.

Responsibilities

• Under supervision, coordinates aspects of patient involvement for complex and/or multiple studies from study initiation until study completion.
• Organizes research information for clinical trials.
• Observes subjects and assists with data analysis and reporting.
• Schedules the collection of data.
• Reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately.
• Monitors, and reports research data to maintain quality and compliance.
• Performs administrative and regulatory duties related to the study as appropriate.
• Participates in other protocol development activities.
• Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
• Educates potential participants and caregivers on protocol specific details and expectations.
• Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
• Assists Clinical Trial Manager (CTM) with oversight of vendors, accounting, regulatory, client satisfaction, recruitment, quality, and trial outcomes.
• Assists the CTM in planning, creating processes, trainings and development of staff.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Skills

Leadership

Mentorship

Communication

Education

High school diploma or equivalent

Bachelor’s degree preferred

CCRC certification preferred

Job description

CenExel is seeking a Clinical Research Coordinator I to coordinate all aspects of clinical trials with strict adherence to ICH, GCP, and protocol guidelines. Located in Marlton, NJ, you will support study initiation through completion, collaborating with investigators, vendors, and sponsors to ensure data quality and participant safety.

The role requires strong communication, leadership, and problem-solving skills, with a focus on regulatory compliance, data integrity, and efficient study