Clinical DM

Adaptivesensorytech; München; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Benefits dieser Stelle

Flexible work-from-home arrangements

Competitive salary

Zusammenfassung

Adaptive Sensory Technology in Munich seeks a Clinical Data Manager to review and process data from global clinical trials, resolve queries with trial sites, and coordinate data transfers with sponsors in accordance with Good Clinical Practice.

You will document your work meticulously, communicate effectively with large pharmaceutical companies, and contribute to improving data quality that underpins trial outcomes and patient health. Flexible work-from-home arrangements are offered.

Qualifikationen

• Experience in handling data from clinical trials and ensuring data quality.
• Ability to resolve data queries with trial sites and sponsors.
• Familiarity with Good Clinical Practice (GCP) standards.

Aufgaben

• Review and process incoming data from global clinical trials.
• Resolve queries in collaboration with trial sites and coordinate data transfers with sponsors.
• Document work according to Good Clinical Practice.

Kenntnisse

Clinical data management

Attention to detail

Communication skills

Jobbeschreibung

Adaptive Sensory Technology was founded by a team of Harvard Medical School scientists, digital photography entrepreneurs, and Google employees. Our motto is "smarter testing for better health" and we are building a platform for intelligent medical devices and data analytics with a focus on ophthalmological solutions.

Our first product already has received regulatory approval and is in use in clinical trials by major pharma companies in North America and Europe. We are now poised to grow our portfolio of digital solutions to transform ophthalmological care.

What we are looking for

Clinical Data Manager (f/m/d)

for our German office in Munich.

As a Clinical Data Manager, you will review and process incoming data from global clinical trials.You will resolve queries in collaboration with trial sites and coordinate data transfers with studysponsors. You will document your work according to Good Clinical Practice.

Who you are

You have strong attention to detail and are passionate about the data quality that ensuresoptimal clinical trial outcomes and thus affects the health and lives of countless patients.

You have excellent communication skills and can professionally and empathetically interact withlarge pharmaceutical companies and with busy clinical trial sites throughout the world.

English is the working language of our multinational team with offices in California and Germany.

What we offer

With a small team, we validated our technology and established ourselvesas a quality leader in the clinical trials market, serving most of the largest pharmaceutical companies in the world.

Joining our team at this stage is a unique opportunity to put your mark on thegrowth of a company, and to positively impact the lives and health of millionsof people. You will have ample room to broadly develop your skills.

We are offering a competitive salary and flexible working-from-homearrangements.