Global Clinical Research Associate

Company Overview

Bristol Myers Squibb (BMS) is a business built around discovering, developing, and delivering medicines for major diseases. They focus on areas such as oncology, haematology, immunology, cardiovascular disease, and neuroscience. BMS believes in meaningful work, high standards and a healthy work culture.

Their India team in Hyderabad is a part of a broader global engine for clinical drug development. That matters for candidates looking for global clinical trial associate jobs in Hyderabad. It means the work sits close to study execution, collaboration, and global clinical trials systems.

BMS focuses on balance, flexibility, inclusion, and growth. It highlights opportunities uncommon in scale and scope. BMS promotes a healthy workplace environment. It is where people bring their own perspective without losing sight of accountability and integrity.

For someone trying to build a future in clinical research operations, this is the kind of environment that can sharpen judgment quickly. You are close enough to the study process to understand what actually keeps trials on track, but not so deep in one narrow task that the learning stops. That is one reason global trial associate jobs in Hyderabad remain attractive for early- and mid-career talent.

Job Summary

This role supports the operational side of global clinical studies. Your work helps the Global Trial Lead keep execution moving, especially when a study needs planning support, documentation control, vendor coordination, and quick follow-through on routine issues. The job exists because studies rarely fail for one dramatic reason. More often, they slow down because smaller operational pieces are not tracked well enough, and this role helps prevent that.

You will handle a mix of project support, study maintenance, file management, meeting coordination, and vendor-related follow-up. Some studies will be simple. Others, especially those in closure, will demand more attention to accuracy and timing. If you are exploring global clinical trial associate jobs in Hyderabad, this is a practical entry into the real mechanics of study management rather than a purely theoretical clinical research role.

Key Responsibilities

• Support study execution using performance metrics and quality indicators.
  You will help the Global Trial Lead track about the status of the study. QC from time to time keeps the team grounded in facts instead of assumptions.

• Handle routine operational issues. Escalate the important ones early.
  Some problems can be resolved within the team. Others need prompt escalation. A good trial associate knows the difference. He/she/they does not wait too long when a study risk starts to grow.

• Work closely with cross-functional study teams.
  You will be part of the day-to-day conversation with people across the study structure. That makes communication skills an integral part of of the job.

• Maintain study tools, trackers, and project files.
  You will help keep study-level documentation current, which is often where teams lose time if records fall behind. Clean files and current trackers make handovers and reviews far smoother.

• Support eTMF accuracy and completion.
  Trial master file work can look repetitive. But it is one of the first things auditors notice when something is missing. Your role helps keep the archive complete and usable.

• Assist with vendor invoices, accruals, and scope changes.
  Clinical operations is not only science. There are also budgets, approvals, and vendor movement. You will help make sure everything is in line.

• Coordinate meeting agenda, minutes, and follow-up items.
  A lot of trial progress happens between meetings. Your MOM is the key for concrete work. Ensure you document it well.

• Lead or support study closure and archive activities.
  When a study winds down, the pace can get messy if records, site lists, and filing are not handled carefully. You will help close that loop properly so the study can be archived without loose ends.

Qualifications and Skills

Must-Have Qualifications

• BA, BS, or associate degree in a relevant discipline

• 2–4 years of experience using CTMS and TMF systems preferred

• Clinical research or related work experience is a plus

• Basic knowledge of ICH/GCP and regulatory guidance expected

Bonus Skills

• Experience with global study coordination

• Exposure to trial budgets, vendor payments, and accrual tracking

• Comfort with SharePoint, study directories, and site lists

• Understanding of study closure workflows and audit support

Soft Skills & Personality Traits

• Clear communicator

• Organised under pressure

• Quick to learn without becoming careless

• Comfortable asking questions when a process is unclear

• Reliable when deadlines are fast approaching

Salary, Bonuses, & Compensation

You can earn a salary between ₹8 LPA and ₹14 LPA. It will depend on your skills and work experience about how much you'll withdraw.

Alongside pay, BMS highlights competitive benefits, flexibility, and development support. The company also helps employees grow across work and personal life stages.

Location

It is a full time role based in Hyderabad, Telangana, India.

Career Growth Opportunities

Can you contribute positively to the team throughout your tenure? Then, you can be sure of your growth further. You can get into senior trial operations, global study coordination, clinical project management, or broader clinical development support. It is a solid route for people who want to stay in the research ecosystem and move closer to study leadership.

Team Structure

You will support clinical research teams globally. Facilitate projects across internal and external stakeholders. The job is built around coordination instead of just execution.

Why This Role Stands Out

This opening stands out because it sits at the centre of trial execution without asking you to be the entire machine. You get exposure to study planning, closeout, vendor work, eTMF, and stakeholder communication in one role. That combination is rare. It gives you a much clearer picture of how global clinical research actually runs.

How to Apply

Are you looking for a job that utilises your potential in clinical trials? Then, this role is perfect for you. Handle documentation, deadlines, and cross-functional coordination without any issue.

Hit the Apply button to apply to this job. But before that, ensure your CV is updated and optimised. Use keywords like CTMS, TMF, study support, vendor coordination, reporting, or any clinical research.

All the best!!