Call Center Representative (2nd Shift - Mon-Fri 11:30am-8:00pm) - Richmond, Virginia
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Celerion
Richmond, VA, US
Summary
The representative will handle inbound and outbound calls regarding tobacco study participation and manage participant data in the computer system. Additionally, they will promote study participation and conduct reminder calls for registered participants.
Job Description
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Celerion is currently seeking a Call Center Representative to join our Richmond, Virginia team! Do you enjoy providing excellent customer service? If so, we may have the position for you!
We have a Part-time benefitted position available that will work 30-35 hours per week.
In this role, you will answer inbound calls and make outbound calls to/from the public interested in information regarding tobacco study participation. Other duties include collecting and entering participant information into our computer database system, promoting additional study participation and referrals from current study participants, and making reminder call-outs to study participants that are registered for screenings.
Available Schedule:
This position will be scheduled Monday-Friday between the hours of 11:30 am - 8:00 pm.
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Requirements:
- High School diploma or equivalent required
- Must demonstrate excellent communication skills
- Must demonstrate commitment to providing outstanding customer service
- Able to sort information and interpret written and verbal instructions
- Accuracy and attention to detail
- Previous Call Center experience preferred
- Data entry experience preferred
- One year sales, telemarketing, promotional, public relations or related experience preferred
- Ability to work in required work environment, including but not limited to exposure to second hand smoke from combustible cigarettes and vapors from electronic cigarettes on a daily basis
- According to the Code of Virginia 18.2-371.2B, employees must be 21 years of age to work around tobacco products.
\n$18 - $18 an hour\n
Celerion Values: Integrity Trust Teamwork Respect
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
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Celerion, a leader in early clinical research, delivers Applied Translational Medicine. Celerion applies our expertise and experience to translating information gained in research discoveries, to knowledge of drug action and effect in humans to support early drug development decisions and the clinical pharmacology labeling of new medicines.
With over 50 years of experience and 600 global clinic beds (including 24 in-hospital), Celerion conducts and analyzes First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME and NDA-enabling clinical pharmacology studies. Celerion provides expertise on modeling and simulation, study design, medical writing (protocols and reports), clinical data sciences, biostatistics, and PK/PD analysis as well as small and large molecule bioanalytical assays through clinical drug development. Regulatory, drug development and program management complement Celerion’s service offerings.
Our operations are strategically located in:
Lincoln, Nebraska (Corporate Headquarters)
Philadelphia, Pennsylvania
Phoenix, Arizona
Belfast, Northern Ireland,UK
Zurich, Switzerland
Vienna, Austria
Richmond, Virginia
Montreal, Quebec, Canada
For more information, visit: www.celerion.com
Founded
2010
Company size
1,001-5,000 employees
Industry
Pharmaceutical Manufacturing
Org type
Privately Held
Headquarters
Lincoln, NE
Celerion, a leader in early clinical research, delivers Applied Translational Medicine. Celerion applies our expertise and experience to translating information gained in research discoveries, to knowledge of drug action and effect in humans to support early drug development decisions and the clinical pharmacology labeling of new medicines.
With over 50 years of experience and 600 global clinic beds (including 24 in-hospital), Celerion conducts and analyzes First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME and NDA-enabling clinical pharmacology studies. Celerion provides expertise on modeling and simulation, study design, medical writing (protocols and reports), clinical data sciences, biostatistics, and PK/PD analysis as well as small and large molecule bioanalytical assays through clinical drug development. Regulatory, drug development and program management complement Celerion’s service offerings.
Our operations are strategically located in:
Lincoln, Nebraska (Corporate Headquarters)
Philadelphia, Pennsylvania
Phoenix, Arizona
Belfast, Northern Ireland,UK
Zurich, Switzerland
Vienna, Austria
Richmond, Virginia
Montreal, Quebec, Canada
For more information, visit: www.celerion.com
Founded
2010
Company size
1,001-5,000 employees
Industry
Pharmaceutical Manufacturing
Org type
Privately Held
Headquarters
Lincoln, NE