Research Assistant
Tampa, FL Tampa, FL Full-time Full-time From $18 an hour From $18 an hour 9 days ago 9 days ago 9 days ago GENERAL SUMMARY OF DUTIES - Entry level position that provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and FCR guidelines, regulations, and policies.
We have different shift options for this opportunity:
Monday-Wednesday from 6am-6pm and Thursday from 6am-12pm (Inpatient) Monday-Wednesday from 6pm-6am (Inpatient) Monday-Thursday from 7am-5pm (Outpatient) JOB DESCRIPTION Entry Level Position DUTIES INCLUDE, BUT ARE NOT LIMITED TO:
Creating and maintaining screen books and 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 Other duties as assigned KNOWLEDGE, SKILLS & ABILITIES - This position requires the following requirements:
Interest in and knowledge of specific study indications Excellent computer skills Advanced knowledge of electronic equipment (i.
e.
, e-mail, computer, fax machine, copier, etc) Skill in organization and record maintenance Skill in developing and maintaining effective working relationships with supervisors and co-workers Strong personal initiative Ability to complete paperwork with precision 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 A successful candidate will be responsible for ensuring Participants, Sponsors, and Staff is cared for by following the guidelines provided by Management.
The ideal candidate will be a detail-oriented individual that is adaptable to change and has a strong background in Supervision and Organizational Success.
The ideal person is a team player able to work in a fast-paced environment and is willing to adhere to the guiding principles of FCR.
Service Excellence:
We believe all relationships with co-workers, sponsors, and subjects are partnerships.
We demonstrate service excellence through a personal commitment to producing high quality, high-value work, and delivering on time and on target results for every partner.
Safety:
We believe that physical and psychological safety is foundational for a healthy organization.
We proactively identify and mitigate safety risks as part of our daily work and value those who speak up for safety.
Resilience:
We believe resilience is critical for doing our best work.
We demonstrate resilience by remaining flexible, adapting to sudden change, and bouncing back from difficult situations with grace and confidence.
Team Orientation:
We believe that having a team orientation leads to individual and organizational success.
We demonstrate team orientation by working collaboratively and leveraging collective knowledge, ideas, and strengths to achieve a common goal.
Ethical Behavior:
We believe the pillars of ethical behavior are integrity, honesty, respect, courtesy, and caring.
We demonstrate ethical behavior by modeling professional standards of conduct.
Mutual Respect:
We believe that mutual respect cultivates a supportive workplace.
We demonstrate mutual respect by embracing diverse perspectives, sharing ideas, and trusting in each other's abilities.
Open Communication:
We believe that open communication results in a rich and rewarding dialogue that allows for the flow of energy and creativity.
We demonstrate open communication by listening for understanding, speaking up without fear, freely sharing experiences, and soliciting ideas and opinions from others.
EDUCATION - BA/BS preferred or 1-year experience in clinical research preferred EXPERIENCE - One (1) year experience in clinical research is preferred but not required CERTIFICATE/LICENSE - CPR training provided.
Other training such as ECG collection and phlebotomy will be provided on an as-needed basis.
PHYSICAL DEMANDS/WORKING CONDITIONS - Research Assistants may be required to complete job-related tasks outside of that time frame in excess of a standard 40-hour workweek.
Requires prolonged walking, standing, some bending, stooping, and stretching.
Requires hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment.
Requires normal range of hearing and eyesight to record, prepare and communicate appropriate reports.
Requires occasional lifting of boxes up to 50 pounds.
Work is performed in a medical office environment and includes exposure to blood-borne pathogens and bio-hazardous materials.
This role requires the ability to work with a broad range of personalities, situations, and psychiatric disorders; therefore, candidates must possess the ability to resolve conflicts immediately and diffuse potentially escalating events before they occur.
Job Type:
Full-time Pay:
From $18.
00 per hour
Benefits:
401(k) Dental insurance Flexible spending account Health insurance Health savings account Life insurance Paid time off Referral program Vision insurance Schedule:
10 hour shift 12 hour shift Day shift Overnight shift Ability to commute/relocate:
Tampa, FL 33613:
Reliably commute or planning to relocate before starting work (Required)
Experience:
Clinical trials:
1 year (Preferred) Research:
1 year (Preferred) Work Location:
In person Creating and maintaining screen books and 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 Other duties as assigned Interest in and knowledge of specific study indications Excellent computer skills Advanced knowledge of electronic equipment (i.
e.
, e-mail, computer, fax machine, copier, etc) Skill in organization and record maintenance Skill in developing and maintaining effective working relationships with supervisors and co-workers Strong personal initiative Ability to complete paperwork with precision 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 401(k) Dental insurance Flexible spending account Health insurance Health savings account Life insurance Paid time off Referral program Vision insurance 10 hour shift 12 hour shift Day shift Overnight shift Tampa, FL 33613:
Reliably commute or planning to relocate before starting work (Required) Clinical trials:
1 year (Preferred) Research:
1 year (Preferred).
Estimated Salary: $20 to $28 per hour based on qualifications.
We have different shift options for this opportunity:
Monday-Wednesday from 6am-6pm and Thursday from 6am-12pm (Inpatient) Monday-Wednesday from 6pm-6am (Inpatient) Monday-Thursday from 7am-5pm (Outpatient) JOB DESCRIPTION Entry Level Position DUTIES INCLUDE, BUT ARE NOT LIMITED TO:
Creating and maintaining screen books and 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 Other duties as assigned KNOWLEDGE, SKILLS & ABILITIES - This position requires the following requirements:
Interest in and knowledge of specific study indications Excellent computer skills Advanced knowledge of electronic equipment (i.
e.
, e-mail, computer, fax machine, copier, etc) Skill in organization and record maintenance Skill in developing and maintaining effective working relationships with supervisors and co-workers Strong personal initiative Ability to complete paperwork with precision 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 A successful candidate will be responsible for ensuring Participants, Sponsors, and Staff is cared for by following the guidelines provided by Management.
The ideal candidate will be a detail-oriented individual that is adaptable to change and has a strong background in Supervision and Organizational Success.
The ideal person is a team player able to work in a fast-paced environment and is willing to adhere to the guiding principles of FCR.
Service Excellence:
We believe all relationships with co-workers, sponsors, and subjects are partnerships.
We demonstrate service excellence through a personal commitment to producing high quality, high-value work, and delivering on time and on target results for every partner.
Safety:
We believe that physical and psychological safety is foundational for a healthy organization.
We proactively identify and mitigate safety risks as part of our daily work and value those who speak up for safety.
Resilience:
We believe resilience is critical for doing our best work.
We demonstrate resilience by remaining flexible, adapting to sudden change, and bouncing back from difficult situations with grace and confidence.
Team Orientation:
We believe that having a team orientation leads to individual and organizational success.
We demonstrate team orientation by working collaboratively and leveraging collective knowledge, ideas, and strengths to achieve a common goal.
Ethical Behavior:
We believe the pillars of ethical behavior are integrity, honesty, respect, courtesy, and caring.
We demonstrate ethical behavior by modeling professional standards of conduct.
Mutual Respect:
We believe that mutual respect cultivates a supportive workplace.
We demonstrate mutual respect by embracing diverse perspectives, sharing ideas, and trusting in each other's abilities.
Open Communication:
We believe that open communication results in a rich and rewarding dialogue that allows for the flow of energy and creativity.
We demonstrate open communication by listening for understanding, speaking up without fear, freely sharing experiences, and soliciting ideas and opinions from others.
EDUCATION - BA/BS preferred or 1-year experience in clinical research preferred EXPERIENCE - One (1) year experience in clinical research is preferred but not required CERTIFICATE/LICENSE - CPR training provided.
Other training such as ECG collection and phlebotomy will be provided on an as-needed basis.
PHYSICAL DEMANDS/WORKING CONDITIONS - Research Assistants may be required to complete job-related tasks outside of that time frame in excess of a standard 40-hour workweek.
Requires prolonged walking, standing, some bending, stooping, and stretching.
Requires hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment.
Requires normal range of hearing and eyesight to record, prepare and communicate appropriate reports.
Requires occasional lifting of boxes up to 50 pounds.
Work is performed in a medical office environment and includes exposure to blood-borne pathogens and bio-hazardous materials.
This role requires the ability to work with a broad range of personalities, situations, and psychiatric disorders; therefore, candidates must possess the ability to resolve conflicts immediately and diffuse potentially escalating events before they occur.
Job Type:
Full-time Pay:
From $18.
00 per hour
Benefits:
401(k) Dental insurance Flexible spending account Health insurance Health savings account Life insurance Paid time off Referral program Vision insurance Schedule:
10 hour shift 12 hour shift Day shift Overnight shift Ability to commute/relocate:
Tampa, FL 33613:
Reliably commute or planning to relocate before starting work (Required)
Experience:
Clinical trials:
1 year (Preferred) Research:
1 year (Preferred) Work Location:
In person Creating and maintaining screen books and 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 Other duties as assigned Interest in and knowledge of specific study indications Excellent computer skills Advanced knowledge of electronic equipment (i.
e.
, e-mail, computer, fax machine, copier, etc) Skill in organization and record maintenance Skill in developing and maintaining effective working relationships with supervisors and co-workers Strong personal initiative Ability to complete paperwork with precision 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 401(k) Dental insurance Flexible spending account Health insurance Health savings account Life insurance Paid time off Referral program Vision insurance 10 hour shift 12 hour shift Day shift Overnight shift Tampa, FL 33613:
Reliably commute or planning to relocate before starting work (Required) Clinical trials:
1 year (Preferred) Research:
1 year (Preferred).
Estimated Salary: $20 to $28 per hour based on qualifications.
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