• Job Description

  Req#: R359684

  Job Description

  About the Position

  We are currently seeking a skilled and motivated Associate Clinical Research Associate (aCRA) to join our team. Together, we share a mission to execute clinical research in an innovative, efficient, quality-focused, and compliant manner to improve and save lives worldwide.

  As an aCRA, you will play a vital role in ensuring excellence in clinical trials and site performance. Clinical research is a cornerstone of our business, and you will carry significant responsibility as the primary site contact and site manager for assigned protocols and sites. Reporting to a CRA Manager, you will gain an in-depth understanding of study protocols and procedures, perform clinical study site management and monitoring activities, and develop strong, lasting relationships with clinical sites throughout all phases of the trial.

  About You

  We are looking for a proactive and adaptable colleague who thrives in a fast-paced environment and embraces challenges. You will be part of a positive, experienced team and contribute by sharing best practices and recommending continuous improvements.

  Core Competencies:

  • Fluent in Norwegian and English with excellent communication skills, including the ability to understand and present technical information clearly.
  • Solid understanding and working knowledge of clinical research, clinical trial phases, and current GCP/ICH guidelines as well as Norwegian clinical research laws.
  • Strong IT skills, including proficiency in MS Office and various clinical IT applications across computer, tablet, and mobile devices, with the ability to quickly adapt to new technologies.
  • Solution-oriented mindset with the ability to manage complex issues effectively.
  • High sense of ownership, accountability, and urgency, with excellent prioritization skills to handle multiple tasks in a dynamic environment.
  • Ability to work effectively in a multicultural environment and establish culturally sensitive working relationships.
  • Willingness and ability to travel domestically and internationally approximately 50% of the time.
  • Valid driver’s license.

  Experience & Education Requirements

  • Minimum of two years’ experience in clinical research.
  • Bachelor’s degree with a strong emphasis on science and/or biology.

  Why Join Us?

  You will be part of a global leader in healthcare innovation, working alongside passionate professionals dedicated to advancing clinical research and improving patient outcomes. We offer a supportive environment that fosters growth, learning, and career development.

  How to Apply

  If you are ready to contribute to meaningful clinical research and grow your career, please submit your application, including your CV and cover letter, through our career portal.

  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:

  Domestic/International

  VISA Sponsorship:

  No

  Travel Requirements:

  50%

  Flexible Work Arrangements:

  Remote

  Shift:

  Not Indicated

  Valid Driving License:

  Yes

  Hazardous Material(s):

  n/a

  Required Skills:

  Accountability, Adverse Event Report, Clinical Evaluation Reports, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Testing, Clinical Trial Planning, Clinical Trials Monitoring, Data Analysis, Good Clinical Data Management Practice (GCDMP), Investigations Training, Key Stakeholder Relationships, Management Process, Protocol Adherence, Regulatory Compliance, Root Cause Analysis (RCA), University Education

  Preferred Skills:

  Job Posting End Date:

  08/17/2025

  *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.

• About the company

  Merck & Co., Inc.,

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