Merck & Co, Inc

Clinical Research Manager (CRM) Lead - Lung

Merck & Co, Inc • $142K — $224K *
Rahway, NJ 07065In-Person
Pharmaceuticals & Biotech
8 - 10 years of experience
Today
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Job Overview by Ladders

Qualifications

  • 10+ years of clinical research experience with increasing responsibilities, including 5+ years of leading projects and teams
  • Bachelor's degree in Science or a comparable field
  • Knowledge of ICH GCP and local regulations in clinical trials
  • Strong project and site management skills, proven through successful implementation
  • Effective communication abilities in English and local language with stakeholders

Responsibilities

  • Lead one or several therapeutic areas (TAs) within the country's clinical trial portfolio
  • Ensure successful execution, enrollment, and quality of clinical trials
  • Develop operational strategies and quality plans for all programs in the TA portfolio
  • Collaborate with local and regional stakeholders to build principal investigator networks
  • Oversee performance management and career development of the clinical research team

Benefits

  • Remote work flexibility
  • Opportunities for career development and mentorship
  • Dynamic role with significant impact on clinical research strategy
  • Involvement in cross-functional collaboration and global initiatives
  • Access to a growing portfolio of clinical trials and therapeutic areas
Full Job Description
Job Description

This role will be key to further develop the country capabilities in clinical research. Under the direction of the country or cluster CRD/TA-Head the person will be responsible for the end-to-end performance of clinical trials in 1 or several Therapeutic Areas (TA), from feasibility to close out in 1 or several countries. The role will be responsible for oversight of the employees working in the TA, with line management of CRMs and functional oversights of other roles in their studies. At the discretion of the CRD/TAHead, the role could also be responsible for direct project work and will ensure excellent study performance with strict adherence to local regulations, our company SOPs and ICH GCP.

As line manager the role is critical to develop key talents in the organization to ensure a pool of successors in critical roles.

The role will work at country level with other local stakeholder like GMA, GHH, PV and regulatory to ensure alignment and development of the country capabilities and collaborates and works closely with other stakeholders in the TA in GCTO & GCD.

Responsibilities include, but are not limited to:
  • Will lead 1 or several TA of the growing portfolio in the country.
  • Accountable for the successful execution, enrollment and quality of their clinical trial portfolio
  • Accountable to ensure performance metrics, timelines and key milestones are met in compliance with ICH/GCP and country regulations, our companie's policies and procedures, quality standards and adverse event reporting requirements internally and externally.
  • Accountable to develop operational strategies and quality plans for the conduct of all programs and studies in the TA portfolio.
  • Collaborates with other TA directors, local and regional stakeholder in GCTO in order to develop and build territory of principal investigators and sites.
  • Ensures oversight and line management of Clinical Research Manager (CRM) team.
  • Oversee the performance management and career development of staff and effectively manage performance issues.
  • Lead a team independently with supervision from CRD/TAH to high performance.
  • Accountable for CRM performance reviews, including addressing low performance situations, and taking appropriate actions.
  • Ensures key talent development and retention.
  • Collaborates internally with the cross-functional teams on local, regional and global level.
  • Collaborates externally with investigators, regulators and vendors
  • Supports strategic initiatives across country, Global Clinical Development GCD and GCTO
  • Supports local strategy development consistent with long-term corporate needs in conjunction with CRD.
  • Together with direct reports contributes significantly to effective conduct of clinical studies and to develop the pipeline, while maintaining regulatory requirements and compliance
  • Main Point of Contact (POC) for assigned protocols and link between Country Operations and Clinical Trial Team (CTT).
  • Responsible for project management of the assigned studies: pro-actively plans, drives and tracks execution and performance of deliverables/timelines/results to meet country commitments from feasibility and site selection, recruitment, execution and close out.
  • Reviews Monitoring Visits Reports and escalates performance issues and training needs to CRA-Manager and/or functional vendor and internal management as needed. Performs Quality control visits as required.
  • Leads local study teams to high performance: trains in the protocol other local roles, closely collaborates with and supports CRAs as protocol expert and coordinates activities across the different local country roles ensuring a strong collaboration (including the CTCs, CRAs and COMs).
  • Responsible for creating and executing a local risk management plan for assigned studies.
  • Ensures compliance with CTMS, eTMF and other key systems in assigned studies.
  • Escalates as needed different challenges and issues to TA-Head/CRD/CCQM and or CTT(as appropriate).
  • Identifies and shares best practices across clinical trials, countries, clusters.
  • May act as a mentor.
  • Responsible for collaboration with functional outsourcing vendors, investigators, other external partners in assigned studies.
  • Country POC for programmatically outsourced trials for assigned protocols.
  • As a customer-facing role, this position will build business relationships and represent our company with investigators and medical centers.
  • Serves local business needs as applicable in his/her country (if delegated can sign contracts and manage budgets).
  • Supports local and regional strategy development consistent with long-term corporate needs in conjunction with CRD, TA-Head and Regional Operations.


Extent of Travel: up to 30% of working time

Skills:
  • Expertise in project and site management. The position requires demonstrated successful implementation of project management skills at program and site level.
  • Strong organizational skills with demonstrated success required.
  • Requires ability to make decisions independently and oversee important activities relevant to clinical research activities according to predetermined global policies and commitments
  • Requires a complete understanding of ICH GCP and global/regional/local regulatory environment.
  • Strong scientific and clinical research knowledge is required. Including extensive knowledge of regional and/or country clinical trial landscape.
  • Deep understanding of our Research and Development division organizational structure and cross-functional roles and responsibilities of its members.
  • Strong understanding of clinical trial planning, management and metrics is essential as well as the ability to focus on multiple deliverables and execute complex protocols simultaneously.
  • Experience functioning as a key link between Country Operations and Clinical Trial Teams.
  • Communicates effectively and fosters a collaborative spirit in a remote/virtual environment and across countries, cultures and functions.
  • Ability, experience, and skills to proactively manage resource allocation, processes (and controls), productivity, quality and project and/or program delivery.
  • Oversee TA strategy alignment and consolidate relevant information, within specific indications, escalating to the TA-H / CRD accordingly.
  • Proficiency in written and spoken English and local language. The incumbent must be competent and effective in written and verbal communication.
  • Strategic thinking.
  • Ability to work efficiently in a remote and virtual environment.
  • The position requires proven strong project management skills and/or project management certification or relevant training program/close mentoring.
  • High emotional intelligence
  • Ability to focus on multiple deliverables and protocols/projects simultaneously.
  • Exercise strategic thinking and executes effectively across projects.
  • Cultivates intercultural understanding.
  • Strong leadership skills that enable and drive alignment with the goals, purpose and mission of our Research and Development division, Global Clinical Development (GCD) and GCTO.
  • Ability to identify problems, conflicts and opportunities early and lead, analyze and creatively prepare mitigation plans and drive conflict resolution is critical.
  • Required to negotiate skillfully in tough situations with both internal and external groups; settle differences with minimum disruption. Examples of common problems include: 1) low patient recruitment, 2) inadequate staff to meet business needs, 3) performance or compliance issues, 4) working with regulatory issues and the broader organization, and5) resolution of conflictive situations.
  • Educational/pedagogic, diplomatic and empathic skills to effectively build and maintain professional relationships with investigators and other stakeholders.


Qualification & Experience:

Required:
  • 10+ years of experience in clinical research with demonstrated success and increasing responsibilities of which 5+ years consisted of leading projects and teams.
  • Bachelor degree in Science (or comparable).


Preferred:
  • CRA Experience preferred.
  • Lung experience preferred.
  • Advanced degree (e.g. Master's degree, MD, PhD).

# eligibleforERP

Required Skills:
Clinical Trial Management, Clinical Trials Operations, Cross-Cultural Awareness, Oncology Trials, People Leadership

Preferred Skills:

Employee Status:
Regular

Relocation:
No relocation

VISA Sponsorship:
No

Travel Requirements:
25%

Flexible Work Arrangements:
Remote

Shift:
1st - Day

Valid Driving License:
No

Hazardous Material(s):
N/A

Job Posting End Date:
08/22/2026
*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.

About Merck & Co, Inc

Schering-Plough Corporation is a major U.S.-based manufacturer of pharmaceuticals. It operates in three segments: Prescription Pharmaceuticals, Animal Health, and Consumer Health Care. Schering-Plough develops products targeting on allergy, cancer, hepatitis, cardiovascular, central nervous system, respiratory system, and more.  It was founded in 1851 by Ernst Christian Friedrich Schering as Schering AG in Germany. Schering-Plough manufactured several pharmaceutical drugs, the most well-known of which were the allergy drugs Claritin and Clarinex, an anti-cholesterol drug Vytorin, and a brain tumor drug Temodar. It also developed drugs targeting on central nervous system and the respiratory system. Schering Plough also owned and operated the major foot care brand name Dr. Scholl's and the skin care line Coppertone. These also became a part of the new company. Schering-Plough was a full member of the European Federation of Pharmaceutical Industries and Associations (EFPIA), a membership which is also maintained by the new Merck.

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Learn more about Merck & Co, Inc
Size
68,000 employees
Market Cap
$282.6 billion
Industry
Pharmaceuticals & Biotech
Net Income
$7 billion
Founded
1668
5 Year Trend
+4.1%
Revenue
$47.9 billion
NASDAQ
MRK
* Ladders Estimates

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