Home
Communities
Companies
- Companies
  
  Discover best places to work
- Compare Companies
  
  Compare & find best workplace
- Add Office Photos
  
  Bring your workplace to life
- Add Company Benefits
  
  Highlight your company's perks
Reviews
- Company reviews
  
  Read reviews for 6L+ companies
- Write a review
  
  Rate your former or current company
Salaries
- Browse salaries
  
  Discover salaries for 6L+ companies
- Salary calculator
  
  Calculate your take home salary
- Are you paid fairly?
  
  Check your market value
- Share your salary
  
  Help other jobseekers
Interviews
- Company interviews
  
  Read interviews for 40K+ companies
- Campus placements
  
  Interviews questions for 1K+ colleges
- Share interview questions
  
  Contribute your interview questions
Jobs
Awards

WINNERS AWAITED!
- ABECA 2025
  
  WINNERS AWAITED!
  
  AmbitionBox Employee Choice Awards - 4th Edition
- ABECA 2024
  
  AmbitionBox Employee Choice Awards - 3rd Edition
- AmbitionBox Best Places to Work 2022
  
  2nd Edition
- AmbitionBox Best Places to Work 2021
  
  1st Edition

Add office photos

Employer? Claim Account for FREE

Bristol-Myers Squibb

Compare

4.2

based on 116 Reviews

51 Bristol-Myers Squibb Jobs

Medical Science Liaison - Clinical Research (Neurology, Immunology)

BRISTOL-MYERS SQUIBB INDIA PVT.LTD.

4.2

based on 116 Reviews

1-2 years

Bangalore / Bengaluru

1 vacancy

Medical Science Liaison - Clinical Research (Neurology, Immunology)

Bristol-Myers Squibb

posted 1d ago

Job Role Insights

Flexible timing

Key skills for the job

Cron Pharmacovigilance Healthcare Clinical Research Clinical Data Management CRM

+ 2 more

Job Description

Title: Medical Science Liaison - Clinical Research

Therapy area - Neurology, Immunology

Location: Field Based (Bangalore)

Role Summary:

Clinical Research Medical Science Liaison (CR-MSL) embodies our medical mission in becoming a trusted, agile partner who engages in relevant dialogue with investigators and delivers timely, high impact data and insights that advance the science and accelerates patient enrolment in clinical trials. CR-MSL is a field-based role with up to 80% time spent in field. CR-MSL will closely collaborates with CR-SMA, RCO and CRC/CRA to develop strategy and drive Phase 1-3 clinical trial activities as per plan.

The primary role of MSL is to identify, develop and maintain contacts with Thought Leaders (TL) and Healthcare Providers (HCP) within therapeutic areas. This role focuses on key investigational programs for respective therapeutic area in which India is a participating country. Within the clinical research remit, this MSL role supports priority studies in respective therapeutic area and engages in peer-to-peer scientific engagement with principal investigators and thought leaders across the country.

Key Responsibilities

External Environment and Customer Focus

Identification and recommendation of top investigators for therapeutic area. Develop and maintain strong working relationships with key Thought Leaders in a disease area, gathering insights on current and future disease management and scientific perspectives including unmet clinical needs. Help understand insights gathered from scientific conversations to inform medical activities and clinical research locally and globally, as well as internal stakeholders where appropriate.
Engage in scientific dialogue around current and emerging data through field visits, presentations, and discussions and at scientific congresses and become the trusted scientific partner for HCPs.
MSL will discuss ongoing clinical trial protocol, MOA of drug and pipeline of therapeutic area if HCP is interested

Support Clinical Trial Activities

Understanding of all current BMS India clinical trials, protocol and MOA drug and therapeutic landscape.
Regular site visits for priority studies & reporting novel insights from trial sites (e.g. barriers to recruitment, change in personnel, competing studies)
Reactive peer-to-peer scientific discussion on relevant congress data and treatment landscapes with key thought leaders
Interaction and medical insight reporting through relevant CRM and reporting tools.
Support Interventional and Non-Interventional Research (NIR) studies (e.g. identification and assessment of potential study sites) to support patient recruitment and/or discussions around the safe and effective use of BMS investigational products, as agreed with local medical management and as defined by the study scope document.
Provide recommendations and insights to clinical development team on study and site feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators, as agreed with local medical management.
Actively support CRO sponsored studies as agreed with local medical management and as defined by the study scope document.
Support HCPs in the ISR submission process as agreed with local medical management and regular follow up on these ISR.
Ensure that BMS Pharmacovigilance procedural documents are understood and applied by investigators of local studies, and alert appropriate BMS personnel to any identified Adverse Events.
Developing/Supporting trial recruitment & internal/external educational initiatives for therapeutic area
Provide support/participation in field visits of global team, HO initiated R&D days, advisory board meetings, investigator or Site engagement meetings
MSLs can build partnerships and advocacy and bring back insights on clinical trial designs, patient experiences, and unmet medical needs to R&D and Medical Affairs

Provide Medical Support

At all times, MSLs will perform their activities in an ethical and compliant manner, acting with the highest integrity in adherence with all BMS policies and external laws and regulations.

Models a strong work ethic and consistently achieves results in line with BMS Values by demonstrating a high level of personal motivation and commitment.
Acts purposefully and demonstrates dedication to advance the MSL value proposition toward strategic outcomes by taking innovative action.
Looks for ways to succeed in line with BMS values regardless of the challenge.
Shares best practices to optimize team performance and is viewed as a role model for overcoming obstacles, challenges, and development opportunities.
As necessary and appropriate, support the initial and ongoing medical/scientific area and product specific training and provide key scientific updates to internal stakeholders (e.g. RCO, CRC, CRA, Regulatory, Pharmacovigilance).

The profile of an MSL is complementary to those of CRAs tracking and reporting site recruitment, optimizing referral and trial awareness with little overlap. Good communication and understanding of the different profiles and tasks and close collaboration and alignment will be mandatory

Qualifications

MBBS, MD, BDS, MDS
1-2 years of experience in a medical, scientific and/or clinical research environment
Discussing scientific or clinical data and collect medical insights from healthcare professionals.
Effectively listening, communicating, and presenting scientific and/or clinical data to research or healthcare professionals
Developing peer-to-peer relationships with top-ranking doctors, scientists or other healthcare professionals
Training others
Quickly and comprehensively learning about new subject areas and environments
Ability to travel up to 80% of workdays.

Languages

Excellent English language skills - spoken and written.

Experience And Knowledge

Working in a scientific and/or clinical research environment
Ability to work independently and act as a team player.
Have an innovative mindset and approach.
Translating scientific or clinical data into an understandable and valuable form to help physicians best serve their patients.
Good communication and presentation skills to present scientific and/or clinical data to research or healthcare professionals
Developing peer-to-peer relationships with TLs, scientists, and other healthcare professionals
Ability to learn about new subject areas and environments quickly and comprehensively.
Disease area knowledge and an understanding of scientific publications
Knowledge of clinical trial design and process
Knowledge of the national healthcare and access environment
Knowledge of HEOR core concepts (Health economic and outcome research) is a plus.