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Associate Director, Study Manager - Atherosclerosis and Metabolism

Job in Rahway, Union County, New Jersey, 07065, USA
Listing for: MSD Malaysia
Full Time position
Listed on 2026-10-09
Job specializations:
  • Healthcare
  • Management
Salary/Wage Range or Industry Benchmark: 142400 - 224100 USD Yearly USD 142400.00 224100.00 YEAR
Job Description & How to Apply Below

Job Description This position participates in the strategy and leads the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to demonstrate your advanced leadership and technical skills as part of a global, cross-functional team. You will build and coach your team in the development of project management, communication, and collaboration skills in support of our clinical trials.

Job Responsibilities
  • Responsible for the operational planning, feasibility, execution and conduct of clinical trial(s).
  • Serves as the Clinical Trial Team (CTT) lead;
    Leads and directs teams in key study planning, development, and execution elements (e.g. operational reviews, issue escalation/mitigations, presentations agement meetings, program level cross functional meetings and governance).
  • Responsible for facilitating and collaborating with key internal/external stakeholders (study team, subsidiary country teams, vendors, committees, etc.) in support of clinical trial objectives.
  • Liaises with partners, vendors, and vendor management team.
  • Review and provide clinical operations input into relevant clinical documents such as the protocol and other documents as appropriate.
  • May serve as a subject matter expert and/or participate on process improvement teams.
  • Builds talent and capabilities of junior team members through proactive coaching, mentoring and development opportunities.
  • May include management of direct/indirect reports including assignment of resources, professional development, and performance management.
Core Skills
  • Strong knowledge of clinical research regulatory requirements e.g., Good Clinical Practice (GCP) and International Council for Harmonisation (ICH)
  • Proven ability to manage competing priorities and effectively delegate and assign activities to meet the business needs
  • Ability to develop short and mid-range project plans that are realistic and effective at meeting goals
  • Strong analytical skills to drive operational milestones
  • Influence opinions and decisions of internal and external customers/vendors, across functional areas, and within the division
  • Interact with key stakeholders across department, division, and company.
  • Role requires a proactive approach, strategic thinking and leadership driving toward study goals.
  • Demonstrated leadership skills in programs & processes, leading meetings and influencing peers and direct/indirect reports in a matrix environment.
  • Problem solving, prioritization, conflict resolution, and critical thinking skills
  • Strong communication, writing, and presentation skills
  • Proficient knowledge in Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.)
Education/Experience
  • Bachelor's Degree and 9+ years of pharmaceutical, clinical drug development, project management, and/or medical field experience
    -OR
    - Master's Degree and 6+ years of pharmaceutical, clinical drug development, project management, and/or medical field experience
    -OR
    - PhD/PharmD Degree and 2+ years of pharmaceutical, clinical drug development, project management, and/or medical field experience.
  • Degree in life sciences, preferred clinicaltrialjobs
Required Skills
  • Adaptability
  • Analytical Problem Solving
  • Clinical Data Management
  • Clinical Study Management
  • Collaboration
  • Detail-Oriented
  • Ethical Standards
  • Good Clinical Practice (GCP)
  • Stakeholder Alignment
  • Strategic Thinking
Preferred Skills
  • Process Improvements
  • Program Management
  • Project Management

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.

For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment.

We encourage our colleagues to respectfully challenge one another’s thinking and approach problems…

Position Requirements
10+ Years work experience
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