Job Description

Are you passionate about healthcare and innovation? Do you have a detail-oriented mindset and a desire to make a difference in people's lives? If so, we invite you to join us as a Senior Clinical Trial Coordinator. This vital role in our research & development division allows you to contribute directly to our premier mission of delivering innovative health solutions. Your meticulous work will ensure the comprehensive administration of clinical trials and the timely maintenance of tracking and reporting tools.Your Core ResponsibilitiesAs part of your role, you'll manage the comprehensive administration of clinical trials and sites. This includes everything from document tracking and safety report management to database updates.You will have the opportunity to collaborate on the management of clinical and non-clinical supplies, working in conjunction with other team members across various roles.Prepare, distribute, and archive clinical documents, including the responsibility of eTMF reconciliation and ensuring quality control.You'll contribute to site evaluation/validation, startup, and submissions by providing and collecting necessary forms/lists in a timely manner.Exhibit your organizational skills by supporting local investigator meetings.As a process Subject Matter Expert (SME), you'll share best practices, recommend improvements, and provide training to your team members.One of the exciting aspects of this role is the opportunity to mentor junior Clinical Trial Coordinators (CTCs), fostering their professional growth in our company.

Qualifications:

We're seeking candidates who are fluent in local languages and possess business proficiency in English, coupled with excellent communication skills.A good understanding of Global, Country/Regional Clinical Research Guidelines and Good Documentation Practices is necessary for this role.Proficiency in IT skills, including MS Office and clinical IT applications, with a strong focus on MS Excel.Knowledge of ICH-GCP appropriate to the role, accompanied by effective time management, organizational, and interpersonal skills.The ability to thrive in a multicultural environment, with a high sense of accountability and urgency, is vital.We value independent, proactive problem solvers with a positive, growth mindset.A minimum of 3-5 years in Clinical Research or relevant healthcare experience, with completed job training or a Bachelor’s Degree.

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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:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

11/21/2024

*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.

Requisition ID:R320628