Job Description
- Types memos and letters related to research laboratory activities.
- Responsible for daily phlebotomy and specimen processing, and biological sample shipping using universal precautions.
- Uses proper tools and judgment to obtain optimum specimens while minimizing discomfort and hazards for the patient.
- Obtains blood specimens using venipuncture and capillary collections from research patients.
- Exercises judgement within the allowable limits defined within clinical trials protocols, standard operating procedures under the direction from the study Investigator and supervisor.
- Interacts with internal and external personnel to include, but not limited to physicians, nurses, administration staff, industry sponsor representatives, central laboratory/imaging personnel and clinical trial patients.
- Coordinates multiple projects with competing priorities and deadlines as needed based on Clinical Trial Protocol directives and study volume.
- Manage study documentation to include accurate and timely filing.
- Collection of data and date entry.
- Process and ship samples according to all regulations and protocol requirements.
- One year of clinical research or research laboratory preferred.
- Available to travel between San Antonio and Austin site, on an as needed basis.
- Perform other duties as assigned.
Specialized Training:
- GCP training certification preferred
- IATA training certification preferred
Knowledge, Skills, and Other Abilities:
- Demonstrates competence in oral and written communication
- Must be organized, attentive to detail, and possess a positive, friendly, and professional demeanor
- Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
- Requires good medical knowledge, including medical terminology
- Knowledge of CFR, GCP and ICH guidelines required
- Ability to read and comprehend simple instructions, short correspondence, and memos. Ability to write simple correspondence. Ability to effectively present information in one-on-one and small group situations to customers, clients, and other employees of the organization.
- Must have knowledge of Microsoft Office, Microsoft Excel, Internet Explorer, Google Chrome, Mozilla Firefox, and web-based enterprise solutions.
Work Environment and Physical demands:
- Work is performed in an office/laboratory and/or a clinical environment.
- Exposure to biological fluids and/or bloodborne pathogens.
- Personal protective equipment required such as protective eyewear, garments, and gloves.
- Occasional travel may be required domestic and/or international.
- Ability to work in an upright and/or stationary position for 6-10 hours per day.
- Frequent mobility required.
- Occasional squatting, kneeling, or bending.
- Light to moderate lifting and carrying (or otherwise moves) objects including medical equipment with a maximum lift of 20-50 lbs.
Perks of working at Pinnacle Clinical Research:
- 401k
- Medical, dental, vision, long term disability, short term disability, FSA, and life insurance
- 3 weeks of paid time off
- 12 paid company holidays
- Tranquility Room
- Pinnacle Gym (San Antonio office)
- Scrub voucher (specific positions apply)
- And more!
Pinnacle Clinical Research is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.
About Pinnacle Clinical Research:
Pinnacle Clinical Research is dedicated to conducting cutting-edge research with a special focus on fatty liver disease (non-alcoholic). We pride ourselves on conducting high quality research as a complement to the medical care that our volunteers receive from their routine care center. Be a part of the discovery!