Research Assistant/Medical Assistant

CenExel; Atlanta (GA); On-site; USD 28,000 - 29,000; Full time

Benefits offered by this job

Health Insurance

Dental Insurance

Vision Insurance

Long-Term Disability

Short-Term Disability

Life Insurance

401k

Job summary

CenExel Clinical Research is seeking a detail-oriented assistant to support CRCs at our Atlanta site. You will manage study-related patient charts, prepare visits, and handle data entry, paperwork, and coordination with participants and vendors.

The role emphasizes accuracy, communication, and teamwork in a fast-paced clinical trial environment. Competitive benefits apply after probationary period.

Qualifications

• Interest in and knowledge of specific study indications.
• Excellent computer skills and advanced knowledge of electronic equipment (e.g., e-mail, computer, fax, copier).
• 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.

Responsibilities

• Create and maintain patient charts for all assigned studies.
• Prepare participant visits per CRCs schedule; manage source documents and lab results in patient charts.
• Maintain inventory of study supplies (lab kits, assessments, and participant materials).
• Complete data entry and resolve CRF queries per sponsor timelines.
• Assist Coordinators with assessments (e.g., blood pressure, urine collection).
• Communicate with study participants, caregivers, vendors, and laboratories as needed.
• Assist Coordinators with scheduling, copying, faxing, and clerical tasks.
• Aid Coordinators in monitoring visits for studies.
• Complete daily responsibilities delegated by CRCs for the study/participants.
• Carry out additional duties as assigned.

Skills

Attention to detail

Communication skills

Organizational skills

Phlebotomy experience

Patient interaction

Relationship building

Calm under pressure

Guideline interpretation

Verbal communication

Tools

Computer literacy

Job description

CenExel ACMR
501 Fairburn Road SW
Atlanta, GA 30331, USA

Description

About Us:

Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

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 depending on experince, education, and skillset.

Essential Responsibilities and Duties:

• Creating and maintaining patient charts for all assigned studies.
• Preparing participant visits based on CRCs 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/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
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