Research Assistant II
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Job Location:
Richfield, MN - USA
Monthly Salary:
$ 16 - 24
Posted on:
11 hours ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Provides lead administrative support to the research site executing and ensuring completion of all
activities of the team by coordinating and assisting patients and visitors visiting the site. Acts as the firstline contact for patients and visitors. Ensures high standards of service and an outstanding patientexperience in relation to communication information and engagement with patients.
Essential Functions:
Coordinates oversees and provides direction for the completion of administrativefunctions on assigned trials.
Welcomes patients and all visitors upon arrival at the site.
Completes data entry and visit completion information and manage the diarysystem ensuring data is accurate and up to date at all times.
Schedules patients for follow-up visits external appointments transport etc.
Conducts reminder telephone calls to patients to confirm visits.
Prepares all relevant patient documentation as per protocol and local regulationsahead of appointment.
May collect medical history information for potential patients liaising withmedical facilities and networks to collect patient files documentation and otherrelevant information as may be required as per protocol.
Collects and tracks patient notes lab results and questionnaires to facilitateprompt reviewing.
Assists with the collection of patient SDV from local medical professional.
Maintains a presentable safe and clean reception area to enhance the patientand visitor experience.
Completes or provides guidance to ensure completion of photocopying faxingpostal activities archiving and patient refreshments.
May provide support in the Pharmacy in all areas of drug administration. Assistswith deliveries checking stock and monitoring inventory of the dispensary.
Assists with collating files counting IP returns and ensuring compliance tocompany SOPs and COPs.
Completes reimbursements of patient study expenses and payments
Collaborates with other site functions to provide accurate and streamlineprocesses and participate in best practice/process improvement initiatives ensuring standardized approach.
Ensures compliance with company quality framework regulatory (GCP)legislation guidelines and international standards (Global/Local COPS & SOPS).
Qualifications:
Education and Experience:
High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification
Technical positions may require a certificate
Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 0to 1 year).
In some cases an equivalency consisting of a combination of appropriate education training
and/or directly related experience will be considered sufficient for an individual to meet the
requirements of the role.
Knowledge Skills and Abilities:
Good understanding of Good Clinical Practices (GCP) with ability to learn and maintain a good working knowledge of FDA regulations and company/client SOPs and WPDs
Solid organizational skills and flexibility to manage workload and meet changing timelines
Firm attention to detail to ensure accuracy and efficiency in data entry
Solid interpersonal/customer service skills positive attitude and good oral and writtencommunication
Capable of working in a team or independently
Solid English language and grammar skills
Good computer skills including proficiency in MS Office (Word Excel and PowerPoint) and basic
understanding of clinical trial database systems
Good analytical and data management skills to effectively analyze data/systems to ensure accuracyand efficiency
BLS or CPR certification
Ability to multi-task and ability to have oversight over a few studies with a number of participants
simultaneously
Strong attention to detail
Working knowledge of medical terminology is an advantage
Compensation and Benefits
The hourly pay range estimated for this position based in Minnesota is $16.10$24.15.This position may also be eligible to receive a variable annual bonus based on company team and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on which includes:
A choice of national medical and dental plans and a national vision plan including health incentive programs
Employee assistance and family support programs including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO) 10 paid holidays annually paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave) accident and life insurance and short- and long-term disability in accordance with company policy
Retirement and savings programs such as our competitive 401(k) U.S. retirement savings plan
Employees Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits please visit: Experience:
Junior IC
Key Skills
- Laboratory Experience
- Spss
- Data Collection
- DNA Isolation
- Stata
- Biochemistry
- Qualitative Research Interviewing
- Research Experience
- Statistical Software
- Molecular Biology
- Research Laboratory Experience
- Western Blot
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
