Assoc. Director Operations Lead

Encontrado en: beBee S CR - hace 1 mes

San Jose, Costa Rica MSD A tiempo completo

Job Description

We are looking for a passionate and experienced leader to join our Global Data Operation (GDO) team as the Associate Director of Clinical Data Management. In this role, you will have the opportunity to drive strategic and tactical operations tasks within our Data Management Center (DMC). Your primary responsibility will be to lead a team of Senior Clinical Data Managers (SCDMs) and Clinical Data Management Analysts (CDMAs), ensuring the consistent execution of quality processes and deliverables.

At our company, our Clinical and Pharmacovigilance teams play a crucial role in conducting high-quality clinical trials that provide the safety and efficacy data necessary for regulatory approval. By integrating cutting-edge technology and adhering to rigorous scientific and ethical standards, we contribute to the development of potential new drugs, vaccines, and indications for existing products.

Key Responsibilities:

  • Direct Line Management: Lead and develop SCDMs and CDMAs, managing their work assignments, conducting skill assessments, providing feedback and coaching, drive annual performance appraisals and ensuring their career development.
  • Process Improvement: Support departmental efforts to simplify and standardize procedures, share best practices, and participate in local and global continuous improvement initiatives.
  • Collaboration and Leadership: Collaborate effectively with business partners to achieve common objectives and participate in cross-functional meetings and initiatives.
  • Training and Development: Train staff on business processes, operations, and tools to enhance their skills and knowledge.
  • Risk Management: Identify and escalate risks and needs to appropriate leadership or management to ensure timely resolution.
  • Business Excellence: Participate in GDO Business Excellence Networks, improvement efforts, and special initiatives as required.

Requirements:

Education: Bachelor's degree in life sciences, computer science, or a related discipline is preferred.

Experience: Minimum of 5 years of experience in Clinical Trials, with at least 2 years of experience in People Management or demonstrated equivalent leadership skills.

Knowledge and Skills: Strong understanding of the end-to-end clinical development process, along with excellent leadership, project management, decision-making, problem-solving, negotiation, and communication skills. Ability to build effective relationships across various business contacts and lead teams with influential and developmental capabilities. Flexibility and adaptability to work under pressure in a dynamic environment.

Join our dynamic team and make a meaningful impact on the advancement of healthcare through clinical data management. Apply now

GlobalDataCR

LaboratoriesLATAM

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:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):


Requisition ID:R284330

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