Clinical Research Associate - CRA (Portugal)

Job Description

We are one of the leading pharmaceutical companies in the world, dedicated to the discovery, development, and delivery of innovative medicines that improve health and quality of life for people. With a strong global presence and an unwavering commitment to scientific research, our mission is to transform health through innovation and excellence in healthcare.We value diversity and inclusion, fostering a collaborative work environment where all employees can contribute their ideas and talents. We believe that our strength lies in the people who are part of our team, and we are constantly looking for passionate and dedicated professionals who want to make a difference.We are recruiting a Clinical Research Associate (CRA) to join our dynamic team in Portugal. This is a unique opportunity for professionals who wish to contribute to the execution of high-quality clinical studies and have a strong interest in driving innovation in the healthcare field. If you are looking for a stimulating and challenging environment where you can grow and develop your career, we are the right place for you.Come be a part of our mission to improve lives around the world!

In our company, the CRA:

• ensures the implementation of clinical trials in compliance with Good Clinical Practices (GCP), Sponsor SOPs, Local Laws and Regulations, Protocol, Monitoring Plan, and associated documents.
• acts as the primary point of contact and manager for the clinical trial at the assigned sites, responsible for overseeing the study conduct throughout all phases, from validation to closure.
• develops close relationships with site teams and ensures the continuity of these relationships throughout all phases of the trial.
• actively collaborates in expanding clinical research activities by identifying and establishing partnerships with new trial sites.
• participates actively in the continuous improvement of processes and systems related to the proper execution of clinical trials.

Availability to travel approximately 65%-75% of the working time (2 to 3 days of travel per week).

Experience and Education:

• Bachelor's degree in a health-related field, with at least 3 years of experience in clinical trial monitoring.
• Fluent in Portuguese and English (spoken and written), with excellent written and oral communication skills.

Skills and Qualifications:

• Solid knowledge of Good Clinical Practices and clinical trial monitoring.
• Experience in conducting clinical trials (validation visits, initiation, ongoing, and closure).
• Ability to manage complex scenarios, working solution-oriented.
• Good IT skills (MS Office) and knowledge of clinical trial management tools.
• Valid driving license.

Behavioral Competencies:

• Proactive, with a positive mindset and problem-solving orientation.
• Responsible and results-focused.
• Detail-oriented and organized.
• Ability to prioritize tasks and manage multiple requests autonomously.
• Good adaptability to a multicultural environment and ability to work in multidisciplinary teams.

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):

Required Skills:

Accountability, Accountability, Adaptability, Adverse Event Reporting System, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Testing, Clinical Trial Planning, Clinical Trials Monitoring, Data Analysis, Data Reporting, Detail-Oriented, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (