Research Assistant I

Posted:
1/28/2026, 7:24:46 PM

Location(s):
Greater Poland Voivodeship, Poland

Experience Level(s):
Junior ⋅ Mid Level ⋅ Senior

Field(s):
Product

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Provides administrative support to the research sites by coordinating and assisting patients visiting the site. Acts as the first-line contact for patients. May assist with patient expense reimbursements and transport arrangements.

Day to day responsibilities:

  • Coordinates and completes administrative functions on assigned trials.

  • Welcomes and assist all visitors upon arrival at the site. Notifies appropriate staff of the visitor's arrival.

  • Prepares and ensures all relevant patient files are ready ahead of the visit as per protocol and local regulations.

  • Completes data entry and visit completion information.

  • Assists with the collection of patient SDV from treating medical professional.

  • Schedules patients for different types of visits, external appointments, transport etc.

  • Conducts reminder telephone calls to patients to confirm visits.

  • Collects, tracks and files patient notes, lab results and questionnaires to facilitate prompt reviewing and able to provide results to patient if required.

  • Maintains a presentable, safe and clean reception area to enhance the patient and visitor experience.

  • Assists with photocopying, faxing, scanning source documents, postal activities, archiving and patient refreshments.

  • Assists with the reimbursement of patient study expenses and payments.

  • Maintains strict confidentiality of patients, employees, customers and company information at all times and adheres to HIPAA Guidelines.

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 0 to 1 year).

Knowledge, Skills and Abilities:

  • Basic understanding of Good Clinical Practices (GCP), with ability to learn and maintain a good working knowledge of FDA regulations and company/client SOPs and SOPs

  • Good organizational skills and flexibility to manage workload and meet changing timelines, handling multiple tasks efficiently and effectively

  • Good attention to detail to ensure accuracy and efficiency in data entry

  • Good interpersonal/customer service skills, positive attitude and good oral and written communication

  • Capable of working in a team or independently

  • Good English language and grammar skills written and verbal

  • Good computer skills, including proficiency in MS Office (Word, Excel, and PowerPoint) and capable of learning new clinical trial database systems

  • Ability to work well in a collaborative team environment

Working Conditions and Environment:

  • Work is performed in an office or clinical environment with exposure to electrical office equipment.

  • Occasional drives to site locations. Potential Occasional travel required.

  • Physical Requirements:

  • Frequently stationary for 4-6 hours per day.

  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.

  • Occasional mobility required.

  • Occasional crouching, stooping, bending and twisting of upper body and neck.

  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

  • Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.

  • May interact with others, relating and gathering sensitive information. Interaction includes diverse groups.

  • Works with guidance or reliance on oral or written instructions from management. May require periods of intense concentration.

  • Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.

  • Regular and consistent attendance.

Thermo Fisher Scientific

Website: https://www.thermofisher.com/

Headquarter Location: Waltham, Massachusetts, United States

Employee Count: 10001+

Year Founded: 2006

IPO Status: Public

Last Funding Type: Post-IPO Debt

Industries: Bioinformatics ⋅ Biotechnology ⋅ Cloud Data Services ⋅ Consulting ⋅ Health Care ⋅ Life Science ⋅ Management Information Systems ⋅ Office Supplies ⋅ Precision Medicine