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Clinical Research Associate (m/w/d)

MSD -
Schwabenheim

Jetzt bewerben

Details zur Stelle

Vollzeit
vor 6 Tagen

Qualifikationen

Englisch
Microsoft Office
Kommunikationsfähigkeit

Vollständige Stellenbeschreibung

Job Description

We are seeking a Clinical Research Associate (m/w/d) to join our team at our innovative research facility in Schwabenheim (near Mainz). This is a full‑time position on a two‑year fixed‑term contract.

Main responsibilities:

Conducting paper and electronic clinical studies under the direction of the Clinical Study Team Leader
Supporting the planning/organization/archiving of clinical studies (field and laboratory studies)
Labelling of investigational products according to Good Manufacturing Practice (GMP)
Organization of logistics for the selected trial veterinarians or laboratories: study product, control product, labelling, study material, study documentation, confidentiality agreements and contracts
Commenting on the study protocol (e.g. practical feasibility, data collection sheets) and the study report
Participation in the study registration/approval for the selected trial veterinarians to the local or federal authorities
Conducting User Acceptance Tests In-house monitoring of clinical studies according to Good Clinical Practice, other guidelines and global or local SOPs, additional monitoring in participating practices in Germany and abroad in Europe.
Conducting protocol training, data entry training in veterinary practices or laboratories
100% review of raw data, inventory of study medication, writing of monitoring visit reports.
Processing queries after data entry and QA audit of raw data
Member of the clinical study team, participation in regular meetings; regular collaboration with other Animal Health R&D sites (e.g. Boxmeer).
Supporting the group with administrative tasks, e.g. orders and billing (ARIBA system)

Your profile:

Scientific degree or completed apprenticeship in a relevant field
Teamwork skills, excellent communication skills and flexibility in an international environment
Careful, structured and results-oriented working style, excellent organization and planning skills
Proficiency in MS Office
Willingness to travel regularly (up to 30%)
Very good English and good German skills, ideally another European language

We are proud to be a company that embraces the value of bringing various, talented, and committed people together. The fastest way to breakthrough innovation is when multiple ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and appreciative workplace.

People with severe disabilities and their equivalents will be given preference if they are equally qualified.

Required Skills:

Adverse Event Report, Clinical Evaluation Reports, Clinical IT, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Management, Clinical Trial Planning, Clinical Trials Monitoring, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (GCP), Investigations Training, Patient Recruitment, Quality Mindset, Regulatory Training

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Project Temps (Fixed Term)

Relocation:

No relocation

VISA Sponsorship:

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

Yes

Hazardous Material(s):

N/A

Job Posting End Date:

06/21/2026

A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID:R398336

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