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구인 뉴욕/뉴저지[2022년 여름] 대학생/성인 파트타임 임상연구 도우미 (6월 초부터)
BY 사운더블헬스2022-05-26 20:48:25
811040

[2022년 여름] 대학생/성인 파트타임 (6월 초부터)

 

(주)사운더블헬스(디지털 헬스 스타트업)에서 파트 타임 임상 연구 도우미(Clinical Research Coordinator)를 구합니다.

 

최소 대학교 2학년 이상인 학생 또는 성인 대상으로 구하고 있으며 의료쪽의 관련 경험을 쌓고 싶은 분들은 좋은

아르바이트 기회 일 듯 합니다.

 

비뇨기과 의료원에서 임상이 진행 될 계획이므로 NJ Englewood에 직접 방문이 가능해야 되고 근무시간은 주로

화요일 - 목요일   오전 9시-오후 5시로 예상합니다. (스케쥴에 따라 오후 1시-5시으로도 운영 가능할 것으로 보임)

 

최소 3주동안 업무를 맡을 수 있는 분을 선호합니다.

 

관심이 있으신 분들은 858-205-7676 또는

alee@soundable.health로 연락을 부탁드립니다.

---------------------------------------------------

[Summer 2022 ] Part-time job for College Students (Starting in June)

 

Part-time Student Clinical Research Worker - Hiring right away

 

Soundable Health, Inc. (digital health startup) is looking for a part time Student Clinical Research Worker.

 

You don’t need a full degree to do this job. We will train you on the first day and the tasks should be easy

enough for you to continue the work by yourself.

 

The job will involve in-person visits to urology clinics or hospitals in NJ Englewood.

The data collection will be conducted in a digital format using iPhones and weight scales.

However, please note that given the nature of the study relating to urination,

you may come across occasions you need to be respectful of study subjects' privacy.

 

A minimum of 3 weeks' commitment would be preferred.

 

Qualifications

  • Minimum 2nd year of bachelor degree [Preferred: currently studying medical or engineering related

  • degree OR prior experience in research or a related field/setting]

  • Must be able to travel to NJ Englewood

  • Punctual

  • Well organized, responsible, and attentive to details

  • Able to understand the clinical research protocol and accurately follow the protocol to manage the study on-site

  • Knowledge of Google/Excel spreadsheets

  • Effective interpersonal skills, including written and verbal communication skills; ability to be with a diverse group

  • of people including physicians, nurses, staffs, scientists, patients and their families

 

Responsibilities

  • Work schedule may vary, but will need to align with the clinical study site schedule between 9am-5pm to maximize data collection

  • It is likely to require commitment on Tuesday 9am-5pm, Wednesday 9am-5pm (or 1pm-5pm), Thursday 9am-5pm (or 1pm-5pm)

  • Tasks involved:

  • Explain the study purpose to the subjects to assist the consenting process

  • Collect the Informed Consent Form with the subjects’ signature

  • Data collection and entry on excel sheet

  • Directly communicate with assigned physicians and subjects

  • Provide direct assistance to the Project Manager in reviewing and verifying the data

  • Set up and teardown the equipment

  • One-time one-to-one onboarding provided

 

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