Alcanza Clinical Research
Data Entry Coordinator - Bilingual required (English/Spanish)
Alcanza Clinical Research, San Juan, San Juan, us, 00902
Data Entry Coordinator - Bilingual required (English/Spanish)
Join to apply for the
Data Entry Coordinator - Bilingual required (English/Spanish)
role at
Alcanza Clinical Research .
Department:
Operations Location:
FDI Clinical Research - San Juan
Alcanza is a growing multi‑site, multi‑phase clinical research company with locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA and Puerto Rico. We have a strong presence across Phase I‑IV studies and therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
Key Responsibilities
In collaboration with other members of the clinical research site team to ensure the entry of clinical visit data in EDC and other clinical data software/systems.
Managing data entry into computer systems for clinical trials, including entering patient data into eDC and other software.
Reviewing patient charts and other medical records to ensure data is entered in a timely manner in accordance with eCRF guidelines and protocol requirements.
Reporting any irregularities or problems with a study to the appropriate parties.
Supporting other clinical research‑related activities.
Ensuring compliance with SOPs, regulations, ICF documentation, and GCP/GDP guidelines.
Maintaining confidentiality of patients, customers, and company information, and performing other related activities as assigned.
Minimum Qualifications
High School diploma or equivalent and a minimum of 1 year of clinical data entry experience, or an equivalent combination of education and experience.
Bilingual required (English/Spanish).
Required Skills
Proficiency with computer applications such as Microsoft applications, email, and web applications; typing proficiency (40+ wpm).
Strong organizational skills and attention to detail.
Well‑developed written and verbal communication skills.
Well‑developed interpersonal and listening skills, and the ability to work well independently as well as with co‑workers, subjects, managers and external customers.
Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
Professional, respectful of others, self‑motivated, and have a strong work ethic.
High degree of integrity and dependability.
Ability to handle highly sensitive information in a confidential and professional manner, in compliance with HIPAA guidelines.
Benefits
Full‑time employees regularly scheduled to work at least 30 hours per week are benefits‑eligible, with coverage starting on the first day of the month following date of hire.
Medical, dental, vision, life insurance, short‑ and long‑term disability insurance, health savings accounts, supplemental insurances, and a 401(k) plan with a safe‑harbor match are offered.
Seniority level:
Entry level
Employment type:
Full‑time
Job function:
Information Technology
Industries:
Research Services
Referrals increase your chances of interviewing at Alcanza Clinical Research by 2x.
#J-18808-Ljbffr
Data Entry Coordinator - Bilingual required (English/Spanish)
role at
Alcanza Clinical Research .
Department:
Operations Location:
FDI Clinical Research - San Juan
Alcanza is a growing multi‑site, multi‑phase clinical research company with locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA and Puerto Rico. We have a strong presence across Phase I‑IV studies and therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
Key Responsibilities
In collaboration with other members of the clinical research site team to ensure the entry of clinical visit data in EDC and other clinical data software/systems.
Managing data entry into computer systems for clinical trials, including entering patient data into eDC and other software.
Reviewing patient charts and other medical records to ensure data is entered in a timely manner in accordance with eCRF guidelines and protocol requirements.
Reporting any irregularities or problems with a study to the appropriate parties.
Supporting other clinical research‑related activities.
Ensuring compliance with SOPs, regulations, ICF documentation, and GCP/GDP guidelines.
Maintaining confidentiality of patients, customers, and company information, and performing other related activities as assigned.
Minimum Qualifications
High School diploma or equivalent and a minimum of 1 year of clinical data entry experience, or an equivalent combination of education and experience.
Bilingual required (English/Spanish).
Required Skills
Proficiency with computer applications such as Microsoft applications, email, and web applications; typing proficiency (40+ wpm).
Strong organizational skills and attention to detail.
Well‑developed written and verbal communication skills.
Well‑developed interpersonal and listening skills, and the ability to work well independently as well as with co‑workers, subjects, managers and external customers.
Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
Professional, respectful of others, self‑motivated, and have a strong work ethic.
High degree of integrity and dependability.
Ability to handle highly sensitive information in a confidential and professional manner, in compliance with HIPAA guidelines.
Benefits
Full‑time employees regularly scheduled to work at least 30 hours per week are benefits‑eligible, with coverage starting on the first day of the month following date of hire.
Medical, dental, vision, life insurance, short‑ and long‑term disability insurance, health savings accounts, supplemental insurances, and a 401(k) plan with a safe‑harbor match are offered.
Seniority level:
Entry level
Employment type:
Full‑time
Job function:
Information Technology
Industries:
Research Services
Referrals increase your chances of interviewing at Alcanza Clinical Research by 2x.
#J-18808-Ljbffr