Global Trial Acceleration Associate at Bristol-Myers Squibb

Hyderabad, Telangana, India

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Not SpecifiedCompensation

Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

PharmaceuticalIndustries

Requirements

Minimum of a bachelor’s degree in legal, life science, business administration, or equivalent experience
Advanced degree a plus

Responsibilities

Manage and execute centralized activities in support of global trials with an emphasis on clinical documentation
Interact with clinical study sites, CROs/vendors, Country Trial Managers (CTM)/Clinical Trial Monitors (CTMo.), the study team, and other functional areas within BMS
Provide support to the Study Team throughout the study duration (start-up, maintenance, and close-out of clinical studies)
Act as the main point of contact for essential document management, ethical, and regulatory submission-related activities
Develop and maintain collaborative working relationships with relevant stakeholders
Support outsourcing activities by interfacing with operational teams, support groups, and service providers for successful selection, contracting, and execution of outsourced studies while ensuring compliance with regulatory standards, ethical practices, BMS outsourcing, and procurement policies and procedures
Initiate and manage start-up documentation activities for global clinical trials
Submit potential investigators to CTSS for debarment review and track decisions
Manage country/site activation for clinical trials as applicable per region, including final review of applicable documents and final sign-off of the country/site activation checklist
Activate sites in accordance with all applicable global/local study procedures
Provide a level of quality control of start-up activity
Update and review various study-related clinical systems (e.g., CTMS, eTMF, or corresponding vendor systems) to determine and report status of clinical trial documents for insourced studies
Arrange certified translation of study level documentation from translators as requested (e.g., ICF, Protocol, IB)
Assist with the coordination or creation of other study-specific materials such as pharmacy or Investigator site file to ensure availability on site for site initiation visits/prior to first patient visit
Act as single point of contact for the study team for centralized activities during study start-up
Perform ongoing maintenance and tracking of essential documentation, collection of updated/outstanding documentation, and submission as required during all phases of clinical trial
Maintain ongoing communication with study teams regarding centralized study activities
Create and manage standardized document templates
Assist with CSR distribution
Handle country and site level ICF adaptation
Collect, review, and approve country and site level essential documents
Centrally review all Site Monitoring Visit reports, issue escalation, resolution, and follow-up tasks
Perform other duties as assigned to support Clinical Trials

Skills

Key technologies and capabilities for this role

Clinical DocumentationEssential Document ManagementRegulatory SubmissionsEthical SubmissionsCRO ManagementVendor ManagementOutsourcingComplianceStakeholder ManagementProcurement Policies

Questions & Answers

Common questions about this position

What are the key responsibilities of the Global Trial Acceleration Associate?

The role involves managing centralized activities for global trials with emphasis on clinical documentation, interacting with sites, CROs, and study teams, handling ethical/regulatory submissions, supporting outsourcing, and managing start-up documentation including country/site activation.

Is this a full-time position?

Yes, this is a full-time employment opportunity.

What is the company culture like at Bristol Myers Squibb?

The culture is described as challenging, meaningful, and life-changing, with uniquely interesting work, opportunities to grow alongside high-achieving teams, and a focus on work-life balance and flexibility.

What benefits does Bristol Myers Squibb offer?

The company offers a wide variety of competitive benefits, services, and programs to help employees pursue their goals at work and in personal lives.

What kind of experience makes a strong candidate for this role?

Strong candidates will have experience in clinical trial documentation, regulatory submissions, site activation, outsourcing with CROs/vendors, and maintaining relationships with stakeholders in global clinical studies.

Bristol-Myers Squibb

Develops and delivers biopharmaceutical medicines

About Bristol-Myers Squibb

Bristol Myers Squibb (BMS) develops and delivers medicines aimed at treating serious diseases, focusing on areas like cancer, autoimmune diseases, and heart conditions. The company conducts extensive research and development to create new drugs, which are sold after receiving regulatory approval. BMS also produces generic drugs, offering affordable alternatives that meet the same quality standards as their branded counterparts. What sets BMS apart from competitors is its dual focus on both innovative and generic medicines, enhancing access to healthcare. The company's goal is to improve patient outcomes while maintaining a commitment to sustainability and corporate responsibility.

New York City, New YorkHeadquarters

1887Year Founded

$33,706.1MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Flexible Work Hours

Hybrid Work Options

Professional Development Budget

Risks

Increased competition in oncology from emerging biotech firms like ArsenalBio.

BMS's lawsuit over the 340B Drug Pricing Program may lead to regulatory challenges.

Rapid AI and digital tech evolution may pose integration challenges for BMS.

Differentiation

BMS focuses on innovative cancer treatments through collaborations like ArsenalBio for T cell therapies.

The company emphasizes digital health technologies, enhancing clinical trial management and patient engagement.

BMS offers both innovative and generic medicines, increasing affordable healthcare solutions.

Upsides

BMS's partnership with Medidata enhances clinical research processes and patient outcomes.

The collaboration with AI Proteins advances novel miniprotein-based therapeutics, expanding therapeutic modalities.

BMS's global license agreement with BioArctic expands its portfolio in neurodegenerative diseases.

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