What are the responsibilities and job description for the Med Info Spec I-Pharm- RTP or Wilmington, NC Hybrid! position at myGwork - LGBTQ Business Community?
This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ business community. Please do not contact the recruiter directly.
Work Schedule
Other
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific team, you’ll discover impactful work, innovative thinking and a culture dedicated to working the right way, for the right reasons - with the customer always top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, and supporting our customers’ medical related inquiries. As the world leader in serving science, with the largest investment in R&D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions. Our commitment to our colleagues across the globe is to provide the resources and opportunities they need to make a difference in our world while building a fulfilling career with us.
This is a hybrid role that requires 1 day in the office per week, in either the RTP or Wilmington, NC locations. Easy driving distance is required.
What will you do in this role?
As Medical Information Specialist, you will have 2 main responsibilities. First, is providing medical and technical information to healthcare providers and patients regarding our client's products. You might answer inquiries about dosage, formulation, indications, or any listed side effects. And for the second part, you will be handling adverse event and/or product complaint reports. You will be responsible for capturing important information related to the adverse event or product complaint and appropriately sharing that information with the client per approved procedures.
A Day In The Life
Responds accurately and professionally to technical and medical information inquiries received via phone, email, internet or mail in reference to pharamaceutical products or devices. Processes fulfillments and provides clinical trial information where appropriate.
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 compaints 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 proceedures 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, research medical literature and drafts responses for such inquiries.
Education Requirements
Bachelor’s degree in pharmacy or equivalent and relevant formal academic / vocational qualification. Some programs may require a Pharm.D.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Experience Requirements
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5 years).
North Carolina active pharmacist license is required.
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role
Knowledge, Skills, Abilities
Excellent verbal and written communication skills.
Excellent language skills (comprehension, speaking, reading and writing).
Proficient computer and keyboarding skills.
Good interpersonal skills.
Ability to work independently as well 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.
Proactive approach to problem solving and decision making.
Ability to motivate, mentor, and provide guidance to less experienced staff.
Advanced critical thinking and problem solving skills with ability to evaluate and escalate appropriately.
Location: Hybrid in RTP or Wilmington, NC areas. Relocation assistance is NOT provided.
Apply today! http://jobs.thermofisher.com
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.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
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.
Work Schedule
Other
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific team, you’ll discover impactful work, innovative thinking and a culture dedicated to working the right way, for the right reasons - with the customer always top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, and supporting our customers’ medical related inquiries. As the world leader in serving science, with the largest investment in R&D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions. Our commitment to our colleagues across the globe is to provide the resources and opportunities they need to make a difference in our world while building a fulfilling career with us.
This is a hybrid role that requires 1 day in the office per week, in either the RTP or Wilmington, NC locations. Easy driving distance is required.
What will you do in this role?
As Medical Information Specialist, you will have 2 main responsibilities. First, is providing medical and technical information to healthcare providers and patients regarding our client's products. You might answer inquiries about dosage, formulation, indications, or any listed side effects. And for the second part, you will be handling adverse event and/or product complaint reports. You will be responsible for capturing important information related to the adverse event or product complaint and appropriately sharing that information with the client per approved procedures.
A Day In The Life
Responds accurately and professionally to technical and medical information inquiries received via phone, email, internet or mail in reference to pharamaceutical products or devices. Processes fulfillments and provides clinical trial information where appropriate.
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 compaints 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 proceedures 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, research medical literature and drafts responses for such inquiries.
Education Requirements
Bachelor’s degree in pharmacy or equivalent and relevant formal academic / vocational qualification. Some programs may require a Pharm.D.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Experience Requirements
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5 years).
North Carolina active pharmacist license is required.
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role
Knowledge, Skills, Abilities
Excellent verbal and written communication skills.
Excellent language skills (comprehension, speaking, reading and writing).
Proficient computer and keyboarding skills.
Good interpersonal skills.
Ability to work independently as well 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.
Proactive approach to problem solving and decision making.
Ability to motivate, mentor, and provide guidance to less experienced staff.
Advanced critical thinking and problem solving skills with ability to evaluate and escalate appropriately.
Location: Hybrid in RTP or Wilmington, NC areas. Relocation assistance is NOT provided.
- Must be legally authorized to work in the United States without sponsorship.
- Must be able to pass a comprehensive background check, which includes a drug screening.
Apply today! http://jobs.thermofisher.com
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.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
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.