Research Fellow (Clinical Trials)

Job Summary

Provides direct support to Clinical Research Coordinators in the completion of protocol‑specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.

Compensation

$20-21/h

Essential Responsibilities and Duties

Creating and maintaining patient charts for all assigned studies.

Preparing participant visits based on CRC's schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.

Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.

Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.

Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.

Communicating with study participants, caregivers, third party vendors and laboratories as needed.

Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.

Aiding Coordinators in the facilitation of study monitoring visits.

Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.

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, and Skills

Interest in and knowledge of specific study indications.

Excellent computer skills and advanced knowledge of electronic equipment (i.e., e‑mail, computer, fax machine, copier, etc.).

Skilled in organization and record maintenance.

Phlebotomy experience preferred.

Experience working with patients.

Skilled in developing and maintaining effective working relationships with supervisors and co‑workers.

Strong personal initiative and attention to detail.

Ability to react calmly and effectively in emergency situations.

Ability to interpret, adapt and apply guidelines and procedures.

Ability to clearly communicate both orally and verbally.

Working Conditions

Indoor, Office environment.

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

Lightly active position, occasional lifting of up to 20 pounds.

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.

Equal Opportunity Employer

This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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