Easter Seals Jobs

Clinical Trial Assistant- Intern - 2406200897W

Description

• Site Identification: Support the local study team in performing country and/or site feasibility.

• Trial documentation: Support the preparation of study files and of any other document required pretrial. Study Start Up Activities / Site start-up

• Help LTM/SM/CTA in ensuring that the current versions of the required trial documents, trial-relatedmaterials and supplies are provided to the investigational site within required timeframes, as applicable.

• Support the LTM/SM/CTA in collecting/preparing documents required for study start-up and ECs and/or Health Authorities Submissions.

• Help the SM in obtaining site related trial documents.

• Support the LTM/SM/CTA in collecting and processing as appropriate the IFDF and related documents throughout the trial.

• May assist the LTM/SM/CTA in conducting local investigator meeting or with making arrangements for the investigators participating in an international meeting, as applicable.

• Help in the distribution, collection, reviewing, and tracking of regulatory documents, agreements and training documentation.

• Support LTM/SM/CTA in drug distribution process, where applicable.

• Support LTM/SM/CTA in ensuring that during the trial all relevant trial related documentation is provided to investigators and central / local IEC (if applicable) within the timelines.

• Support the LTM/SM/CTA in maintaining the study files.

• Provide administrative and logistic support to LTM/SM/CTA in tracking of progress of the trial, management of study data, organizing meetings, mailing and correspondence, materials and otherrelevant tasks as appropriate, where applicable.

• Site closure: Provide administrative and logistic support to the LTM/SM/CTA in activities related to study/site closure, as appropriate, and follow up of all items identified, including support in collecting,processing and archiving of study related documents as appropriate.

• Comply with ICH-GCP and all applicable local laws and regulations.

• Maintain communication with relevant parties within and outside the company.

• Actively follow trainings and complies with relevant training requirements to ensure adequate qualification.

Qualifications

• A minimum of a BA or BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience) isrequired.

• Skills set corresponding with 0-2 years relevant clinical trial experience is preferred; however, other relevant

• Proficient in English language.

• Strong knowledge with MS Office (Word, Excel, Access, Outlook, Explorer andPowerPoint).

• Strong interpersonal and negotiating skills preferred.

• Excellent organizational skills and the ability tocollaborate and handle multiple priorities within a matrix environment.

• Ability to perform activities in a timely and accurate manner.

Primary Location Europe/Middle East/Africa-Israel-Central-Kibbutz Shefayim

Organization J-C Health Care Ltd. (8606)

Job Function Non-LDP Intern/Co-Op

Req ID: 2406200897W