Level

Johnson & Johnson

GCO ED Internship

Johnson & Johnson is hiring a GCO ED Internship. Level rates it ; you can apply on Level.

Level's read on this job

  • On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
  • Tools and skills the posting cites include clinical trials, trial documentation and regulatory compliance.
  • Level files it as an internship.
  • Level lists 2,000+ other open roles at Johnson & Johnson.
  • The role was posted within the past two weeks.

AI in this role

Support clinical trial documentation, study start-up, and regulatory compliance activities as an intern in Neuss, Germany.

clinical-trialstrial-documentationregulatory-complianceadministrative-support

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Career Programs

Job Sub Function:

Non-LDP Intern/Co-Op

Job Category:

Career Program

All Job Posting Locations:

Neuss, North Rhine-Westphalia, Germany

Job Description:

Study Planning Activities


  • Trial documentation: Support the preparation of study files and of any other document required pre-trial.

Study Start Up Activities / Site start-up


  • Support the Trial Manager (TM) or the Site Manager (SM) in EU-CTR Submission Preparation.

  • Help the SM in obtaining site related trial documents.

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

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

Study Execution Activities


  • Support TM/SM in ensuring that during the trial all relevant trial related documentation is provided to investigators and EC (if applicable) within the timelines.

  • Support the TM/SM in maintaining the study files.


Study Close Out Activities


  • Site closure: Provide administrative and logistic support to the TM/SM in activities related to study/site closure, as appropriate, and follow up of all items identified.

General Activities


  • Base all actions on Credo. Protect the rights of others, protect privacy and company assets.
  • Work in line with the HCC, company policies and procedures, including SOPs, having the ethical aspect in mind. Comply with ICH-GCP and all applicable local laws and regulations.
  • Maintain communication with relevant parties within and outside the company.
  • Actively follow trainings to ensure adequate qualification.
  • Regularly update information in applicable systems and templates
  •  Contribute to maintain quality standards and timelines that are consistent with business needs
  • Report every J&J product related complaint you receive to the company, according policies

 

 

Required Skills:

 

 

Preferred Skills:

  

 

The anticipated pay range and benefits for this position is:

Da diese Position in einem Land veröffentlicht wird, das den EU‑Vergütungsanforderungen unterliegt, stellt das Talent Acquisition Team sowohl auf Anfrage als auch allen zu einem Interview eingeladenen Kandidaten Informationen zu den Gehaltsbereichen zur Verfügung.

 

 

How we rate this

GCO ED Internship at Johnson & Johnson rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Clinical TrialsTrial DocumentationRegulatory ComplianceAdministrative Support

Questions you could be asked

  1. Tell me about a project where clinical trials was part of your work. What did you do?
  2. Tell me about a project where trial documentation was part of your work. What did you do?
  3. Tell me about a project where regulatory compliance was part of your work. What did you do?
  4. Tell me about a project where administrative support was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Clinical Trials, Trial Documentation, Regulatory Compliance, and Administrative Support. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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