Senior Clinical Research Associate

<p>Job Description</p><p></p><p><b>Senior Clinical Research Associate (SrCRA)</b></p><p></p><p><b>About the position</b></p><p></p><p>We are currently looking for a highly skilled and motivated SrCRA to share our mission to execute clinical research in an innovative, efficient, high quality and compliant manner to improve and save lives around the world.</p><p></p><p>As a SrCRA you will be employed by Our Company in Sweden and part of an engaged team ensuring excellence in our clinical trials and 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 successful clinical trials. While you as SrCRA will be under the oversight of a Country Lead Clinical Research Manager, you are accountable for performance and compliance for assigned protocols and sites as primary site contact and site manager.</p><p></p><p>Finally, as one of our self-driven and resourceful SrCRAs you will be actively developing and expanding the territory for clinical research – including finding and developing new sites and engaging with internal and external stakeholders.</p><p></p><p><b>About you</b></p><p></p><p>We are looking for a new colleague who is eager to learn and who does not shy away from a challenge. Our new colleague will be part of a fast-paced team full of positive and experienced people. We expect you to contribute strongly to the CRA team knowledge by acting as Subject Matter Expert, sharing best practices, making recommendations for continuous improvement and providing training as <span><span>appropriate/required.</span></span></p><p></p><p></p><p>Furthermore, we are looking for the following core competencies in our new colleague:</p><ul><li>Fluent in both Swedish and English and excellent communication skills, including the ability to understand and present technical information effectively</li><li>Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH, country clinical research law and <span><span>global/country/regional</span></span> clinical research guidelines and ability to work within these guidelines</li><li>Proven skills in site management and monitoring including independent management of site performance and patient recruitment, and professional judgment</li><li>Experience with conducting site motivational visit designed to boost site enrollment</li><li>Advanced 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</li><li>Capable of managing complex issues, works in a solution-oriented manner</li><li>High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment.</li><li>Capable of leading and mentoring CRAs on process/study requirements</li><li>Works effectively in a multicultural environment. Ability to establish and maintain culturally sensitive working relationships.</li><li>Ability to travel domestically and internationally approx. 50% of their working time</li><li>Holds a valid driver’s license</li></ul><p></p><p></p><p><b>Experience Requirements:</b></p><ul><li>Four years of experience with direct site management in pharma/bio/CRO</li><li>Bachelor’s degree with strong emphasis in science and/or biology</li></ul><p></p><p>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.</p><p></p><p>Current Employees apply <a href="https://wd5.myworkday.com/msd/d/task/1422$6687.htmld" rel="noopener noreferrer" target="_blank">HERE</a></p><p></p><p>Current Contingent Workers apply <a href="https://wd5.myworkday.com/msd/d/task/1422$4020.htmld" rel="noopener noreferrer" target="_blank">HERE</a></p><p></p><p><b>Search Firm Representatives Please Read Carefully </b><br/>Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; 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. </p><p></p><p><b>Employee Status: </b></p>Regular<p></p>