Experienced Clinical Research Associate

Posted 6 days ago

This is a fully remote position, open to applicants in Austria.

📋 Description

• Carry out qualification, initiation, monitoring, and closeout visits for research sites in adherence to the approved protocol.

• Engage with medical site personnel, including coordinators, clinical research physicians, and site staff.

• Confirm investigator qualifications, training, resources, facilities, laboratories, equipment, and personnel.

• Validate medical records and research source documentation against case report form data.

• Notify site staff of entry errors and ensure adherence to good documentation practices.

• Communicate protocol deviations in accordance with SOPs, GCP, and relevant regulatory requirements.

• Ensure that investigators enroll only eligible subjects.

• Review regulatory documents.

• Oversee medical device and/or investigational product/drug accountability and inventory management.

• Verify and assess adverse events, serious adverse events, concomitant medications, and related illnesses.

• Evaluate site patient recruitment and retention, providing suggestions for improvements.

• Prepare monitoring reports and follow-up letters that summarize significant findings, deviations, deficiencies, and recommended actions.


⛳️ Requirements

• A minimum of a university degree in a health or life science-related discipline is required.

• At least 1.5 years of prior experience as a Clinical Research Associate (CRA).

• Willingness to travel approximately 60-80% within Germany, Austria, and Switzerland.

• Proficient in Microsoft® Office and possess general computer literacy.

• Exceptional communication and presentation skills.

• Must be detail-oriented and adept at time management.

• Excellent verbal and written communication skills in both English and German.

• Demonstrated experience in clinical patient management, protocol adherence, CRF preparation, and documentation for submission to competent authorities.

• Applications must be submitted in English.


🏝️ Benefits

• Competitive compensation programs that acknowledge and reward performance.

• Comprehensive benefits including health, wellness, retirement, and paid time off (PTO).

• Office-based environment complemented by on-site mentors.

• Clearly defined career paths with opportunities for advancement.

• Industry-leading onboarding and training programs aimed at accelerating professional development.

• Ongoing training and continuous learning opportunities throughout your career.

• A work environment that encourages employees to drive change, share ideas, and grow rapidly.

• Company-sponsored social events.

• Office-based culture with occasional work-from-home flexibility for eligible positions post-training.

People also viewed

ICON plc1 day ago

Senior Clinical Trial Manager – Biotech

RO flagRomania, +11 more countriesFull-timeClinical Research
ApplyView job
ICON plc1 day ago

Senior Clinical Research Associate

ES flagSpain OnlyFull-timeClinical Research
ApplyView job
Parexel1 day ago

Clinical Research Associate I/II – Core Team

AU flagAustralia OnlyFull-timeClinical Research
ApplyView job
Thermo Fisher Scientific1 day ago

FSP CRA, Level II

CN flagChina OnlyFull-timeClinical Research
ApplyView job
Parexel1 day ago

Senior Clinical Research Associate – Core Team

AU flagAustralia OnlyFull-timeClinical Research
ApplyView job
Thermo Fisher Scientific1 day ago

FSP CRA, Level II

CN flagChina OnlyFull-timeClinical Research
ApplyView job

Never miss a great job!

Get handpicked remote jobs straight to your inbox weekly.

Trusted by 7,400+ designers