Clinical Research Coord I na CenExel

Essential Responsibilities and Duties:

 Assists with coordinating all aspects of patient involvement 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.

 Documents adverse events, protocol deviations, and other unanticipated problems

appropriately.

 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).

 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.

Education/Experience/Skills:

 High school graduate or equivalent.

 1 year of experience in clinical research 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.

Working Conditions

1. Indoor, Clinic environment.

2. Shift work, depending on location.

3. Essential physical requirements include sitting, typing, standing, and walking.

4. Lightly active position, occasional lifting of up to 20 pounds. Rarely lift over 20 pounds.

5. Reporting to work, as scheduled, is essential.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.