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(Emmes Group Hiring Global Partnering Associate) |
The clinical research and CRO industry is growing rapidly in 2026, creating high-demand career opportunities for professionals in vendor management, clinical operations, and regulatory compliance. One of the latest opportunities comes from The Emmes Group, a globally recognized Contract Research Organization (CRO), which is hiring a Global Partnering Associate in Bengaluru, India.
This role is ideal for professionals who want to build a strong career in clinical research vendor management, GxP compliance, and global CRO project coordination. It offers exposure to international clinical trials, regulatory frameworks, and collaboration with global stakeholders.
Candidates with experience in clinical operations, vendor management, and project coordination can take advantage of this opportunity to grow in a globally reputed CRO environment.
The Emmes Group is a well-established global CRO known for providing clinical research services, biostatistics, data management, and regulatory support to pharmaceutical, biotechnology, and government organizations.
The company focuses on advancing public health through clinical research and has been involved in multiple global clinical trials across therapeutic areas.
Headquarters
Rockville, Maryland, USA
Founded
1977
Industry
Clinical Research / CRO
Employees
Approximately 1,500+ globally
The Emmes Group is recognized for its strong expertise in clinical trials, regulatory compliance, and data-driven research, making it a preferred partner for global pharmaceutical projects.
The Global Partnering Associate role at Emmes Group is focused on managing and supporting vendor relationships across global clinical trials. This position plays a critical role in ensuring that vendors comply with GxP guidelines and regulatory standards.
The selected candidate will work closely with project managers, quality assurance teams, and external vendors to ensure the smooth execution of clinical trial activities. This includes vendor selection, onboarding, compliance tracking, and performance management.
This job is highly strategic as it directly impacts clinical trial timelines, regulatory compliance, and overall study success.
Company
The Emmes Group
Job Title
Global Partnering Associate
Location
Bengaluru, Karnataka, India
Employment Type
Full-Time
Industry
Clinical Research Organization (CRO)
Work Model
Hybrid / Remote flexibility (as per company policy)
The Global Partnering Associate will be responsible for managing vendor-related activities in clinical research projects.
The role involves identifying and selecting qualified GxP vendors who can support clinical trials effectively. The candidate will also handle vendor onboarding processes, including documentation, compliance checks, and coordination with internal teams.
Maintaining an updated vendor database is an important part of this role. The candidate must ensure that all vendor records are accurate and aligned with regulatory requirements.
The role also includes coordinating Non-Disclosure Agreements (NDAs) and working with legal and contracts teams to finalize vendor agreements.
Collaboration with Quality Assurance teams is required to support vendor audits and ensure compliance with global regulations such as GDPR and the UK Bribery Act.
Additionally, the candidate will participate in RFP processes, manage vendor performance, resolve escalations, and contribute to process improvements through feedback and reporting.
Candidates must meet the following qualifications to apply for this CRO job.
Bachelor’s Degree
B.Pharm / B.Sc / Life Sciences (Mandatory)
Preferred Qualification
M.Pharm or MBA
Additional Certification
PMP Certification (Preferred but not mandatory)
Experience Required
Minimum 4 years of experience in:
Vendor Management
Clinical Operations
Project Management (CRO / Pharma / Biotech)
Candidates applying for this role should possess strong technical and professional skills.
A good understanding of GxP compliance and vendor qualification processes is essential. Candidates should be familiar with clinical trial operations and CRO workflows.
Strong communication and stakeholder management skills are required to coordinate with internal teams and external vendors.
Proficiency in Microsoft Office tools such as Excel, PowerPoint, and Teams is important for reporting and documentation.
Analytical thinking and problem-solving skills are also necessary to handle vendor-related challenges and improve operational efficiency.
The salary for the Global Partnering Associate role depends on experience and skill level.
Estimated Salary Range
₹8 LPA to ₹14 LPA
This range is based on current CRO industry standards in India for mid-level professionals in clinical operations and vendor management.
Additional benefits may include flexible work options, learning opportunities, and career growth in global clinical research projects.
Interview details are not officially specified.
Candidates will be shortlisted based on their resume and experience. Shortlisted applicants may go through multiple rounds, including:
HR Interview
Technical Interview
Managerial Round
Candidates should prepare the following documents before applying.
Updated Resume (CV)
Educational Certificates
Experience Certificates
Identity Proof
Professional Certifications (if any)
Having a well-structured resume increases chances of selection.
Interested candidates can apply through the official application link.
Application Link
Make sure your resume highlights relevant experience in vendor management, clinical research, and regulatory compliance.
The role involves managing vendors, ensuring GxP compliance, and supporting clinical trial operations in a CRO environment.
Yes, a minimum of 4 years of experience in clinical operations or vendor management is required.
The estimated salary ranges between ₹8 LPA and ₹14 LPA depending on experience.
The job is based in Bengaluru, India, with hybrid work flexibility.
The Global Partnering Associate role at The Emmes Group is an excellent opportunity for professionals looking to grow in the clinical research and CRO industry. With strong exposure to global clinical trials, vendor management, and regulatory compliance, this position offers both career stability and growth.
Candidates with experience in clinical operations and GxP compliance should consider applying for this role to gain international exposure and work with a globally recognized CRO.
This job not only enhances technical expertise but also provides opportunities to work on complex global projects, making it a valuable career move in 2026.
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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