Senior Clinical Research Associate

Job Description

Are you a highly skilled and motivated individual looking to make a difference in the field of clinical research? Join our team as a Clinical Research Associate (CRA) or senior Clinical Research Associate (srCRA) and help us execute innovative and high-quality clinical trials to improve and save lives around the world. We are committed to excellence in clinical research, making it a top priority and cornerstone of our business.

Why should you join us?

Join us as a CRA where your growth and professional development is our priority. You'll gain exposure to regional and global assignments, build on your monitoring expertise by contributing to cluster initiatives and have opportunity to progress to other roles within the company. You'll participate in comprehensive training and onboarding programs while representing our company externally, expanding your network and influencing stakeholders. Take the next step in your career with us and make a significant difference in the field of clinical research.

As a CRA, you will work with an engaged team of professionals dedicated to ensuring the success of our clinical trials and site performance. In this role, you will have considerable responsibility and play a vital part in achieving successful outcomes for your study teams and for the CRA team. While working under the oversight of a CRA Manager, you will be accountable for performance and compliance for assigned protocols and sites as the primary contact and site manager.

As a self-driven and resourceful CRA, you will also actively contribute to the development and expansion of our clinical research territory.

About You:

Join a fast-paced team of positive and experienced individuals, where you will have the opportunity to learn and take on new challenges. We are looking for a candidate who can contribute significantly to the CRA team's knowledge by acting as a Subject Matter Expert, sharing best practices, providing recommendations for continuous improvement, and delivering training as needed.

In addition, we are seeking the following core competencies in our new colleague:

• Fluency in both Norwegian and English with excellent communication skills, including the ability to effectively understand and present technical information.

• Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH guidelines, country clinical research laws, and global/country/regional clinical research guidelines. Ability to work within these guidelines.

• Proven skills in site management and monitoring, including independent management of site performance and patient recruitment, and professional judgment.

• Advanced IT skills, including the use of MS Office and various clinical IT applications on different devices (computer, tablet, and mobile).

• Ability to manage complex issues and work in a solution-oriented manner.

• High sense of accountability and urgency. Ability to set priorities and handle multiple tasks in a changing environment.

• Interest in networking and engaging internal and external stakeholder

• Ability to work effectively in a multicultural environment and establish and maintain culturally sensitive working relationships.

• Willingness to travel domestically and internationally approximately 50% of the working time.

• Valid driver's license.

• Minimum two years of experience with direct site management in the pharma/bio/CRO industry for CRA position

• Minimum four years of experience with direct site management in the pharma/bio/CRO industry for senior CRA position

• Bachelor's degree with a strong emphasis on science and/or biology.

Benefits:

• Growth and development opportunities

• Hybrid way of working

• You will have a chance to participate in an annual incentive plan (bonus)

• Car or car allowance as per your choice

• Good pension scheme

We prioritize talent and provide ample opportunities for growth within our organization, fostering a dynamic and collaborative environment that is dedicated to making a positive impact on healthcare outcomes.

To apply, please submit your resume and cover letter highlighting your qualifications and experience in the field of clinical research. We look forward to reviewing your application.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse 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 diverse workplace.

Required Skills:

Accountability, Accountability, Adaptability, Adverse Event Report, Clinical Data Management, Clinical Development, Clinical Research, Clinical Research Organizations (CRO) Management, Clinical Sciences, Clinical Study Management, Clinical Trial Compliance, Clinical Trial Documentation, Clinical Trial Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Customer-Focused, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (GCP), Information Technology (IT) Support, Medical Research, Microsoft Office, Patient Recruitment, Pharmaceutical Management, Site Management {+ 1 more}

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:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

50%

Flexible Work Arrangements:

Remote

Shift:

Not Indicated

Valid Driving License:

Yes

Hazardous Material(s):

n/a

Job Posting End Date:

04/27/2026

*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.