Clinical Research Associate

Allucent; Bengaluru; On-site; INR 1,200,000 - 1,800,000; Full time

Benefits offered by this job

Flexible working hours

Mentoring opportunities

Professional development budget

Buddy program

Growth opportunities

Referral program

Loyalty awards

Job summary

Allucent is seeking a CRA to lead monitoring activities, own sites and investigator relationships, ensuring trial integrity with our collaborative team. You will oversee site initiation, routine monitoring, and close-out visits, while supporting regulatory affairs and start-up processes to ensure compliant study execution.

You should have haemophilia monitoring experience and at least 5 years in monitoring, with strong ICH-GCP knowledge.

Qualifications

• Strong knowledge of ICH-GCP and regulatory guidelines.
• Haemophilia trial experience is a must with monitoring background.
• Experience leading monitoring in complex trials, preferably oncology or rare diseases.
• Willingness to travel as required.

Responsibilities

• Independently manage all aspects of monitoring for assigned trials across study phases.
• Ensure compliance with protocols, ICH, SOPs and regulatory requirements.
• Build strong site relationships and be the primary contact for investigators.
• Identify and resolve site issues to maintain data quality and patient safety.

Skills

ICH-GCP understanding

Regulatory guidelines

Haemophilia monitoring

Oncology/rare disease exp

Travel readiness

Job description

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. At Allucent we are big enough to deliver and small enough to care. We know all our colleagues by name and work together as a team to make everyone SHINE.

The role

As an CRA, you will take the lead on monitoring activities, owning your sites and relationships with investigators. You’ll be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, experienced team. This includes work related to regulatory affairs, site activation processes—including contracting and start-up activities—to ensure smooth and compliant study execution.

Main responsibilities:

• Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
• Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection.
• Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.

· Activities around regulatory affairs, site activation and study-startup.

• Haemophilia trial experience is mustalong with monitoring experience Haemophilia study.
• You’re an experienced CRA ready to take the next step with a company that truly values your expertise and independence. You thrive in an agile, collaborative environment and want to be part of a team making a real impact.
• Experience leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of at least 5 years’ experience.
  • Strong understanding of ICH-GCP and regulatory guidelines.
  • Comfortable working independently and managing priorities.
  • Willingness to travel, as required.

Benefits of working at Allucent include:

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Leadership and mentoring opportunities
• Participation in our enriching Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
• Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees.

About Allucent

Our mission is to help bring new therapies to light. When you work at Allucent, that means applying your unique skill set, expertise, and knowledge to build partnerships with our clients in their pursuit to develop new, life-improving treatments.

If you're passionate about helping customers develop new pharmaceuticals and biologics; have an entrepreneurial spirit; and ready to join other science, business, and operations leaders, we would love to get to learn more about how we can help each other grow.

Together we SHINE. find more information about our values.

Disclaimers:

*Our in-office work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices.

“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”