Junior Clinical Research Associate (Clinical Research Experience Required)

The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development. For those with medical and/or health/life science degree with clinical research experience who want to travel throughout Germany, Austria, Switzerland , and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields.

PACE – MEDPACE CRA TRAINING PROGRAM

Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.

Through our PACE Training Program, you will join other P rofessionals A chieving C RA E xcellence:

• PACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.
• PACE will prepare you by developing your CRA skills through interactive discussions and hands‑on job‑related exercises and practicums.
• To supplement your in‑house and field‑based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.

UNEXPECTED REWARDS

This role will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:

• Dynamic working environment, with varying responsibilities day to day;
• Expansive experience in multiple therapeutic areas;
• Work within a team of therapeutic and regulatory experts;
• Defined CRA promotion and growth ladder with potential for mentoring and management advancements;
• Competitive pay and opportunity for significant travel bonus.

CRA PERKS

• Competitive travel bonus
• Flexible work hours across days within a week
• In‑house travel agents
• Ongoing therapeutic training by our in‑house physicians who are medical and regulatory experts
• Opportunities to work with international team of CRAs

Responsibilities

As a CRA, you will specifically be responsible for the following:

• Conduction of qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
• Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
• Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
• Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
• Verification that the investigator is enrolling only eligible subjects;
• Regulatory document review;
• Medical device and/or investigational product/drug accountability and inventory;
• Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
• Completion of monitoring reports and follow‑up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications

• Must have a minimum of a university degree in a health or life science related field;
• Approximately 60‑80% travel;
• Proficient knowledge of Microsoft® Office and general computer literacy;
• Outstanding communication and presentation skills;
• Must be detail‑oriented and efficient in time management; and
• Excellent verbal and written communication skills in German and English.

We kindly ask to submit your application in English শক্ত।

Medpace Overview

Medpace is a full‑service clinical contract research organization (CRO). We provide Phase I‑IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.Lets leverage local regulatory and therapeutic expertise across all major areas including oncology, cardi(run)/ etc etc etc. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications}.e{' and if interested, you will be contacted with details for next steps.

• Must have a minimum of a university degree in a health or life science related field;
• Approximately 60-80% travel;
• Proficient knowledge of Microsoft® Office and general computer literacy;
• Outstanding communication and presentation skills;
• Must be detail‑oriented and efficient in time management; and
• pull

We kindly ask to submit your application in English.

Responsibilities (repeated)

As a CRA, you will specifically be responsible for the following:

• Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
• Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
• Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
• Verification that the investigator is enrolling only eligible subjects;
• Regulatory document review;
• Medical device and/or investigational product/drug accountability and inventory;
• Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
• Completion of monitoring reports and follow‑up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications (repeated)

• Must have a minimum of a university degree in a health or life science related field;
• Approximately 60-80% travel;
• Proficient knowledge of Microsoft® Office and general computer literacy;
• Outstanding communication and presentation skills;
• Must be detail‑oriented and efficient in time management; and
• Excellent verbal and written communication skills in German and English.

We kindly ask to submit your application in English.