CRA Manager
CRA Manager
MSDFresher
- Posted 22 hours ago
- Be among the first 10 applicants
Job Description
Job Description
This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director, the person is responsible to manage a team of 6-14 CRAs and to ensure excellent study and site performance with strict adherence to local
regulations, company SOPs and ICH GCP.
As line manager the role is critical to continuously develop key talents by providing training,
support and mentoring to the CRAs and properly manage situation of low or non-performance.
The role will work at country level with other local stakeholder e.g. Clinical Research Manager to ensure alignment and development of the country capabilities. The role will collaborate with country Partner Line Managers to ensure alignment across all monitoring functions. The person contributes to Headquarters capacity/resource planning activities to ensure efficient allocation of resources and work.
Responsibilities include, but are not limited to
Adaptability, Adaptability, Clinical Research, Clinical Research Management, Clinical Trial Documentation, Clinical Trial Management, Clinical Trial Planning, Clinical Trials Monitoring, Clinical Trials Operations, Continuous Development, Cross-Cultural Awareness, Decision Making, Ethical Standards, Global Coordination, Good Clinical Practice (GCP), Liaison Work, Oncology Trials, Partner Relationship Management (PRM), People Leadership, Performance Improvements, Policy Compliance, Procedure Adherence, Process Alignment, Process Standardization, Regulatory Compliance + 7 more
Preferred Skills
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)
Job Posting End Date
10/9/2026
This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director, the person is responsible to manage a team of 6-14 CRAs and to ensure excellent study and site performance with strict adherence to local
regulations, company SOPs and ICH GCP.
As line manager the role is critical to continuously develop key talents by providing training,
support and mentoring to the CRAs and properly manage situation of low or non-performance.
The role will work at country level with other local stakeholder e.g. Clinical Research Manager to ensure alignment and development of the country capabilities. The role will collaborate with country Partner Line Managers to ensure alignment across all monitoring functions. The person contributes to Headquarters capacity/resource planning activities to ensure efficient allocation of resources and work.
Responsibilities include, but are not limited to
- Work allocation, staff development and performance appraisal.
- Provides input for capacity planning, including reporting of current manpower and forecasting of CRA capacity and needs, to provide efficient use of resources.
- Work with CRAs, PLMS and other functions to ensure consistency of processes and protocol implementation across the country, to reduce variability and provide predictability.
- Interacts with sites as needed to resolve site or CRA operational issues to meet commitments in a timely manner in coordination with the study CRM.
- Attend local Investigator Meetings if requested to.
- Interface with GCTO partners on clinical trial execution.
- Escalates site performance issues to CRM and Clinical Research Director CRD.
- People and Resource Management
- Manage CRA – career development, performance reviews, etc., including
- Support and resolve escalation of issues from CRAs.
- Liaise with local HR and finance functions as required.
- Contribute to HQ capacity/resource planning activities to ensure efficient allocation of resources and work. Manage local conflicts between resource and work.
- Provides training, support and mentoring to the CRA to ensure continuous development.
- Ensures CRA compliance to corporate policies, procedures and quality standards
Adaptability, Adaptability, Clinical Research, Clinical Research Management, Clinical Trial Documentation, Clinical Trial Management, Clinical Trial Planning, Clinical Trials Monitoring, Clinical Trials Operations, Continuous Development, Cross-Cultural Awareness, Decision Making, Ethical Standards, Global Coordination, Good Clinical Practice (GCP), Liaison Work, Oncology Trials, Partner Relationship Management (PRM), People Leadership, Performance Improvements, Policy Compliance, Procedure Adherence, Process Alignment, Process Standardization, Regulatory Compliance + 7 more
Preferred Skills
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)
Job Posting End Date
10/9/2026
- 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.
More Info
Key Skills
Clinical Trials Monitoring
Cross-Cultural Awareness
Global Coordination
Performance Improvements
Oncology Trials
Ethical Standards
Liaison Work
People Leadership
Clinical Trial Planning
Clinical Trials Operations
Partner Relationship Management PRM
Procedure Adherence
