Job Details

ID #2169343
State Texas
City Galveston
Full-time
Salary USD TBD TBD
Source Texas
Showed 2019-05-06
Date 2019-04-24
Deadline 2019-06-23
Category Healthcare
Create resume

Clinical Research Coordinator (Webster/ Clear Lake, TX)

Texas, Galveston 00000 Galveston USA

Vacancy expired!

Clinical Research Coordinator

Summary: The following responsibilities will be allocated to the Clinical Research Coordinator, however; duties are not limited to this listing only. Additional tasks can be assigned to the employee at the discretion of the Supervisor. Please submit your resume with salary requirements. Do not apply for the position unless you have experience as a Clinical Research Coordinator.

Job Description and Duties:

Coordinates and administers the patient care functions.

Oversees the planning, scheduling, and implementation of day-to-day clinical activities.

Recruitment, screening, enrollment, and retention of clinical research subjects.

Educates subjects on treatment and protocol including benefits and/or risks for participants.

Coordinates and maintains contacts with patients, physicians and sponsors.

Coordinates and monitors the collection, processing, shipping and recording of clinical data and/or specimen samples, as required by established study protocol.

Assure compliance with all requirements for Serious Adverse Event reporting, as well as submission of all required documents for review.

Administers prescribed study medications, performs phlebotomy, monitors vital signs, and/or performs other specialized medical procedures.

Identifies problems and trends, recommending procedural changes to managers.

Directs the work of support staff, laboratory technicians and assistants.

Knowledge, Skills, and Abilities required:

Must have experience as a Clinical Research Coordinator.

Bilingual is preferred (FLUENT IN SPANISH).

Proficient with GCP and Human protection guidelines.

Maintain patient confidentiality.

Organizing, coordinating, and multi-tasking skills.

Ensure proper documentation, adequate supplies, and patient scheduling.

Ability to observe, measure, and record symptoms, reactions, and progress.

Ability to make administrative and procedural decisions on sensitive, confidential issues.

Strong interpersonal and communication skills and the ability to work effectively within a team.

Knowledge of clinical and/or surgical facilities, instruments, and equipment.

Ability to prepare and process laboratory samples using established protocols.

Ability to draw blood, administers IVs, and performs standard nursing procedures.

Ability to learn new software applications for electronic data entry.

Working conditions and physical effort:

Work is normally performed in an outpatient clinic environment.

Training and working at other locations may be required.

No overtime, comp time or mileage reimbursement will be paid.

Some travel to investigator meetings and educational seminars may be required and may include nights and weekends.

Occasionally, employees may be required to work weekends.

Benefits:

23 days paid time off / year (8 company holidays; 15 days for sick/personal use)

Health, Dental and Vision insurance available

401K, Profit-sharing plan and Safe Harbor

Vacancy expired!

Subscribe Report job