Safety Specialist

Thornton Tomasetti; Gurugram District; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Abbott is seeking an individual contributor for clinical affairs responsibilities in India, Gurgaon. The role involves planning timelines, coordinating with cross-functional teams, and ensuring trials adhere to SOPs and GCP guidelines.

Collaborate with project teams to manage budgets and regulatory requirements. The ideal candidate holds a life sciences-related degree with at least two years of clinical research experience, strong communication, and proficient use of Microsoft Office and

Qualifications

• Bachelor’s degree from an accredited university with focus in medicine, life science, nursing, bioengineering or related field.
• Minimum two years of clinical research experience.
• Understanding of medical terminology.
• Strong written and verbal communication, interpersonal, presentation and organizational skills.
• Ability to interpret basic safety data and communicate with all levels of staff.
• Ability to work independently but seek guidance when necessary.
• Ability to exchange information clearly and verify understanding.
• Proficiency in Microsoft Office Suite and relevant clinical applications.

Responsibilities

• Plans, directs, creates and communicates clinical study timelines.
• Gathers input from cross-functional teams to create plans and deliverables on schedule.
• Ensures consistency of clinical study processes across trials.
• Oversees and resolves operational aspects of clinical trials with SOP, GCP and country regulations.
• Ensures study is conducted within clinical trial protocols.
• Monitors progress and follows up with team members and line managers.

Skills

Communication skills

Organizational skills

Independent work

Medical terminology

Microsoft Office

Safety data interpretation

Education

Bachelor’s degree in life sciences or related field

Tools

Microsoft Office Suite

Clinical applications

Job description

JOB DESCRIPTION:

MAIN PURPOSE OF THE ROLE Individual contributor that works under limited supervision. Applies subject matter knowledge. Requires capacity to understand specific needs or requirements to apply skills/knowledge.

MAIN RESPONSIBILITIES

• Plans, directs, creates and communicates clinical study time-lines.
• Gathers input from cross-functional teams and creates plans that help the team produce deliverables on schedule.
• Ensures consistency of clinical study and processes across clinical trials.
• Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations such as site and vendor selection, preparing clinical trial budgets.
• Ensures study is conducted within clinical trial protocols.
• Monitors progress and follows up with team members and line managers when issues develop.

Qualifications: Required:

• A Bachelor’s degree from an accredited university or college with an academic focus in medicine, pre-medicine, nursing, life science, bioengineering, or a related academic field.
• Minimum two years of clinical research experience.
• Understanding of medical terminology.
• Strong written and verbal communication, interpersonal, presentation and organizational skills.
• Has the ability to interpret basic safety data to meet deadlines as well as the ability to communicate effectively with all levels of employees.
• The ability to generally work independently but seek guidance when necessary.
• The ability to exchange straightforward information, ask questions and check for understanding.
• The ability to achieve thoroughness and consideration when accomplishing a task.
• Must be proficient in Microsoft Office Suite and relevant clinical applications.

Qualifications: Desired:

• A general familiarity with clinical trials research processes.
• Previous related experience in research within a clinical or corporate setting or relevant clinical experience in a clinical/hospital environment.
• Work habits include organization, coordination of multiple tasks, accuracy and attention to detail.

The base pay for this position is N/A

In specific locations, the pay range may vary from the range posted.

Job Details

• JOB FAMILY: Clinical Affairs / Statistics
• DIVISION: MD Medical Devices
• LOCATION: India > Gurgaon : BPTP Park Centra
• ADDITIONAL LOCATIONS: (none)
• WORK SHIFT: Standard
• TRAVEL: Not specified
• MEDICAL SURVEILLANCE: Not Applicable
• SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential - because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions - across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health.

An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce.

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