Clinical Research Job at Thermo Fisher Scientific India
Explore a rewarding clinical research job with Thermo Fisher Scientific, a global leader shaping the future of science and innovation. This remote India-based role offers exceptional growth for professionals seeking impactful work in medical projects, clinical safety, and global trial operations. Perfect for those exploring thermo fisher scientific careers or looking to advance in competitive health science jobs, this opportunity provides stability, purpose, and worldwide impact.
Job Details:
- Job Title: Sr Medical Project Coordinator
- Location: Remote, India
- Job Id: R-01318933
- Category: Clinical Research
- Remote: Fully Remote
About the Company
Thermo Fisher Scientific is a global innovation leader committed to enabling customers to make the world healthier, cleaner, and safer. With clinical trials in more than 100 countries and a strong PPD clinical research portfolio, the company offers some of the most promising Thermo Fisher Scientific careers for individuals seeking advancement in science, research, and health science jobs. Team members are empowered with resources, global exposure, and meaningful work that enhances health outcomes worldwide.
Job Description:
Thermo Fisher Scientific is looking for a dedicated Sr Medical Project Coordinator to assist in the management and ongoing evaluation of medical projects for one or more programs in collaboration with management and other stakeholders. This role ensures consistency, alignment, and compliance of internal processes as well as optimal performance and issue resolution throughout the project lifecycle.
Qualifications:
- Education: Bachelors degree in Health Sciences (Physician’s Assistant) or licensed RN
- Experience: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years), including 2+ years of clinical safety experience (clinical research monitoring, pharmacovigilance, or a combination)
Clinical Research Job – Key Responsibilities:
- Coordinates and reviews safety data, utilizing line listings, company dashboard(s), and/or other visualization tools.
- Reviews data for safety trends, coding consistencies, and potential follow-up with investigator sites.
- Identifies potential issues and resolves or escalates as appropriate.
- Reviews safety data and may provide summations for safety review meetings.
- May review designated sections of aggregate reports.
- May help to create/review safety and medical management plan(s) on studies and ensures processes reflect contracted services.
- Assists in routine project implementation, forecasting, coordination, and reviewing metrics and budget considerations.
- Monitors the status of data review and escalates delays and/or risks to all stakeholders.
- May present at business development, client, and investigator meetings and participate in strategy/business development calls.
- Resolves complex problems through in-depth evaluation of various factors and offers solutions.
- May serve as the primary contact for clinical/data management project teams.
- Assists management in training and mentoring.
Clinical Research Job – Knowledge, Skills, Abilities Required:
- Knowledge of GCPs for medical oversight of clinical trials and SAE processing
- Knowledge of drug development and safety reporting
- Knowledge of safety data trending including coding
- Working knowledge of biostatistics, data management, and clinical procedures
- Strong problem-solving and critical thinking skills
- Good oral and written communication skills
- Strong attention to detail
- Ability to work in a collaborative team environment
- Ability to maintain a positive and professional demeanor in challenging circumstances
