Job Description

Senior Clinical Research Associate (SrCRA) for Our Company in Denmark

About the position

We are currently looking for a highly skilled and motivated SrCRA who shares our passion for getting safe and efficient treatment to patients as smoothly as possible. You will be employed by Our Company in Denmark.

As a SrCRA you will be part of a very engaged team ensuring excellent clinical trials and high site performance. Clinical Research at Our Company is given top priority and is a cornerstone of the business. Consequently, you will as a SrCRA have considerable responsibility and play an important part in ensuring compliance of clinical trials.

While you as SrCRA will be under the oversight of a CRA Manager, you, as primary site contact and site manager, claim overall responsibility throughout the whole process.

Finally, as one of our fast-paced and resourceful SrCRAs you will also be actively developing and expanding the territory for clinical research – including finding and developing new sites.

Please apply before 25th April with your resume and cover letter.

About you

We are looking for a new colleague who is eager to learn and who do not shy away from a challenge. Our new colleague would be part of a fast-paced team full of positive and experienced people to learn from.

Furthermore, we are looking for a colleague that:

• Are fluent in both the local language and in English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively
• Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines
• Excellent understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines
• Proven skills in Site Management including independent management of site performance and patient recruitment
• Experience with conducting site motivational visit designed to boost site enrollment
• Demonstrated high level of monitoring skill with independent professional judgement
• Able to work highly independently across multiple protocols, sites and therapy areas
• High sense of accountability/urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment
• Works with high quality and compliance mind-set
• Are good at analyzing data and at seeing challenges where others might see a problem
• Good IT-skills (use of MS office, use of various clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices
• Will be able to travel domestically and internationally approx. 65 percent of their working time (expected travel 2-3 days per week)
• Holds a valid driver’s license

We are looking for a Senior Clinical Research Associate that:

• Have four years of experience with direct site management (monitoring) in pharma/bio/CRO
• Holds a BA in Science and/or Biology

About us

As a workplace, Our Company offers an environment with a high degree of trust and opportunities to grow. We firmly believe in the ability to work as a team, and we pride ourselves in our prioritization of talent. We are a certified Great Place to Work and the social and professional well-being of our employees and colleagues are of the utmost importance.

We aspire to be the premier research-intensive biopharmaceutical company in the world. We demonstrate our commitment to patients and population health by increasing access to health care through far-reaching policies, programs, and partnerships.

Today, we continue to be at the forefront of research to prevent and treat diseases that threaten people and animals – including cancer, cardiometabolic diseases, infectious diseases, Alzheimer’s disease, and infectious diseases including HIV and Ebola. Our purpose is to save and improve lives for generations.

Our strategy is simple: We follow the science. The path to discovery is often unclear, but we are tireless in seeking solutions for some of the world’s most difficult health challenges.

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:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Remote

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

04/26/2025

*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.