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Start-up Specialist (Associate Clinical Operations Manager I)

atMSD (THAILAND) LTD.

Job Description

This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCPand country regulations, policies and procedures, quality
standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. COM, the person is responsible for execution and oversight of clinical trial country submissions and
approvals.

Key responsibilities include:
  • Contribute to Execution and oversight of clinical trial country submissions and approvals for assigned protocols.
  • Develops working knowledge of local language materials including local language Informed Consents and translations. May interact with IRB/IEC and Regulatory Authority for assigned
protocols.
  • Supports country deliverables, timelines and results for assigned protocols to meet country commitments. Responsible for quality and compliance in assigned protocols in country.
  • Contributes to the development of local SOPs.
  • Coordinates and liaises with CRM, CTC, CRA to ensure country deliverables are obtained for submissions, budgets, CTRAs and local milestones.
  • Support local processes, clinical and ancillary supplies management, importing and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention
requirements. Enters and updates country information in clinical and finance systems.
  • Support of local regulatory and financial compliance.
  • Acquire knowledge how to in/directly influence investigators, external partners and country operations
  • Works in partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors
and sites, IRB/IECs and Regulatory Authorities in submission and approval related- interactions with support of an experienced COM. Through continual interaction with local clinical team/s successfully
delivers clinical and financial contracts within fair market value.
  • Contribute to initiatives and projects adding value to the business, as appropriate/required.
  • Contributes to COM team and other Country Operations roles knowledge by acting as/supporting process Subject Matter Expert (SME), sharing best practices, making recommendations for
continuous improvement as appropriate/required.
  • Contributes to COM team knowledge by sharing best practices as appropriate/required

Qualification/Experience & Skills:

  • 2 years of experience in Clinical Research
  • Bachelor's degree in Health Care
  • Basic knowledge of local regulatory environment and submission and approval processes, and understanding of how these impact study start-up.
  • Positive & growth mindset, capable of working independently and being self-driven
  • Ability to propose solutions to local study teams.
  • ICH/GCP knowledge appropriate to role. Hands on knowledge of Good Documentation Practices
  • Able to work with other experienced clinical research professionals to learn and develop skills to manage protocols independently. Works with high quality and compliance mindset.
  • Effective and efficient time management, organizational and interpersonal skills, conflict management and problem-solving skills.
  • High sense of accountability and urgency in order to properly prioritize deliverables
  • Strong communication and negotiation skills in local language and English.
  • Ability to focus on multiple deliverables and protocols simultaneously is essential.
  • Good IT skills and ability to adapt to new IT applications
  • Excellent verbal and written skills, in local language and English
  • Strong coordination and organizational skills

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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:

Shift:

Valid Driving License:

Hazardous Material(s):


Requisition ID:
R259832

Experience required
  • 2 years
Salary
  • Negotiable
Job function
  • Product / Brand Management
  • Assistant
  • Management
Job type
  • Full-time

Company overview

Size:2000-5000 employees
Industry:Advertising / Media
Location:Bangkok
Website:www.merck.com
Founded in:n/a
Ranking:4/5

Merck & Co., Inc. (Merck) is a global research-driven pharmaceutical company that discovers, develops, manufactures and markets a range of products to improve human and animal health. The Company?s operations are principally managed on a products basis and comprises of two business segments: the Pha ... Read more

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