Job Description
Are you passionate about making a difference in the world through research and innovation in the biopharmaceutical industry? If so, we have an exciting opportunity for you to join our research-driven biopharmaceutical company as a Clinical Research Associate (CRA). As a CRA, you will play a crucial role in ensuring the safety and efficacy of our existing and pipeline products, making a significant impact on patients' lives globally.
At our company, we believe that great medicines can change the world. Our mission is to follow the science and invent medicine and vaccine innovations that make a difference. We are dedicated to world-class science and are committed to pushing the boundaries of global healthcare through research and innovation.
Responsibilities
1. Develop strong site relationships and ensure continuity throughout all phases of the clinical research study
2. Conduct site management and monitoring activities in compliance with applicable regulations and protocols
3. Gain an in-depth understanding of the study protocol and related procedures
4. Coordinate and manage various tasks in collaboration with other sponsor roles to ensure site readiness
5. Participate in site selection and validation activities
6. Perform remote and on-site monitoring and oversight activities to ensure the accuracy and completeness of data generated at the site
Qualifications, Experience, And Skills
1. A degree in science or a science-related field
2. Clinical research experience, such as Clinical Trial Assistant, Study Coordinator, or similar roles
3. Direct site management (monitoring) experience in a bio / pharma / CRO company
4. Good understanding and working knowledge of clinical research, including phases of clinical trials, International Conference on Harmonisation - Good Clinical Practice, and country-specific clinical research law and guidelines
5. Familiarity with Global, Country, and Regional Clinical Research Guidelines and ability to work within these guidelines
6. Hands-on knowledge of Good Documentation Practices
7. Valid driver's license and ability to travel domestically and internationally, approximately 65%-75% of working time, with an expected traveling frequency of 2-3 days per week
Why Join Us
1. Be part of a research-driven enterprise dedicated to world-class science and making a significant impact on patients' lives globally
2. Work on innovative medicine and vaccine innovations that have the potential to change the world
3. Join a team of passionate professionals who are pushing the boundaries of global healthcare through research and innovation
4. Enjoy a field-based role that provides the opportunity to travel domestically and internationally
If you are looking for an opportunity to contribute to meaningful research and make a difference in the world, we would love to hear from you. Apply now and become part of our team of Clinical Research Associates pushing the boundaries of healthcare through innovation.
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
Requisition ID: R342852
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