Med Info Spec I (Night Shift & Hybrid) - Clinical Trial Patient Screening | Registered Nurse or Pharmacist Required
- Remote job
JOB DESCRIPTION
Work Schedule
Third Shift (Nights)Environmental Conditions
OfficeJob Description
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
Location/Division Specific Information
Our work is a story of global impact.
Within Medical Communications , we improve patient health by supplying medical information services to our customers, patients and healthcare providers. We engage with healthcare professionals, regulatory agencies and pharmaceutical customers to help them navigate regulatory and compliance requirements around the world. We manage medical information inquiries, document adverse events and product complaints, report product launches, prepare standard responses to inquiries and develop process improvements for customer implementation.
Office Location: Seven/NEO Building, Bonifacio Global City, Taguig City, Philippines
Shift Schedule: NIGHT SHIFT (US business hours; program operates from 8:00 PM to 8:00 AM PHT, with assigned shift from 12:00 AM to 8:00 AM PHT)
Work Setting: Hybrid; once a week on-site
Training Period: 4 to 5 weeks (once a week on-site)
Discover Impactful Work:
Provides technical and medical information, and/or performs intake of adverse events/ product complaints with quality customer service. Analyzes and researches inquiries and documents interactions according to organizational, client and regulatory guidelines. The information provided will be given to a level in parallel with the individual’s expertise, experience and training.
A day in the Life:
Manage high-volume inbound and outbound interactions (calls, emails, and SMS/Chats) with individuals interested in participating in Program/Client clinical trials, including conducting eligibility screening, matching participants to appropriate clinical trials and sites, and completing accurate documentation in a fast-paced environment.
Responds accurately and professionally to technical and medical information inquiries received via phone, email, internet or mail in reference to pharmaceutical or device products. Processes fulfillments and provides clinical trial information or after-hours on-call support.
Analyzes caller’s questions to formulate an accurate and concise response using client
approved resources and records inquiries and interactions in the appropriate databases following organizational, client and regulatory guidelines.
Identifies, records and triages adverse events and product complaints according to organizational, client and regulatory guidelines and provides additional support (including follow up) as needed.
Maintains detailed knowledge of project and corporate policies and procedures including client products, SOPs, protocols, GCPs, and applicable regulatory requirements.
Works closely with internal and external client contacts (up to and including members of client management) to resolve complex inquiries. As needed, researches medical literature and drafts responses for such inquiries.
Keys to Success:
Education
Bachelor's Degree Graduate in any Life Science or Healthcare related Courses (i.e. Pharmacy OR Nursing only)
Active professional license is required.
Experience
Previous clinical research experience is a plus.
Must be a Registered Nurse or Pharmacist with an active license (required)
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
Knowledge, Skills, Abilities
Excellent English verbal and written communication skills (comprehension, speaking, reading and writing); Fluency skills in a second language may be required.
Proficient computer and keyboarding skills
Good interpersonal skills
Ability to work independently and as part of a team.
Ability to interpret client provided complex medical and technical information.
Organizational and time management skills
Ability to maintain a positive and professional demeanor in meaningful circumstances.
Working Environment
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
Able to work upright and stationary for typical working hours.
Ability to use and learn standard office equipment and technology with proficiency.
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
This position is a hybrid position
Training will be 12 weeks on site followed by once per week in office expectations
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Apply today!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Accessibility/Disability Access
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.
This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.
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