Associate Dir/Medical Director - Pulmonary/Critical Care
Job DescriptionAs part of the Thermo Fisher Scientific team, you ll discover meaningful work that makes a positive impact on a global scale.
Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer.
We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Due to continued growth, CRG is now looking to appoint an Associate Medical Director/Medical Director of Pulmonary/Critical Care, to join our team of Medical Directors in North America.
This role can be office-based or home based.
The Associate Medical Director/Medical Director will be responsible for providing medical support and medical advice for clinical trials and safety evaluation within the PPD Pharmacovigilance department.
A day in the Life:
- Provide study, project and program-specific medical monitoring and review services, including but not restricted to:
- Leading of all medical aspects of contracted tasks.
Supervising of safety variables.
- Discussing with clients, investigators and healthcare professionals of medical issues in the pre and post approval services by using accurate medical judgment, interpretation and decision.
- Provide medical consultation to team members and answer study related medical questions.
Communicate clearly with associates and clients, maintaining and open line of communication to ensure all procedures are followed appropriately - Analysis and assessment of safety data to identify and run emerging safety signals.
- Medical review of individual case safety reports, serious adverse event reports and clinical outcome reports.
- Assist in Business Development activities - Present PPD standard medical safety processes to clients at business development meetingsand connect with various medical communities to explore and expand PPD business.
- Participate in training of project teams.
- Provide therapeutic and protocol training as needed.
- Write, review and approve reports, regulatory submissions and protocols, ensuring that the medical content is accurate and complete.
Keys to Success:
Education - MD, MB/BS or equivalent degree and strong medical knowledge, validated clinical experience handling Pulmonary/Critical Care patients in hospital practice - Significant experience within pharmaceutical industry, clinical trials or pharmaceutical medicine is beneficial - Is proficient in spoken and written English - Solid understanding of regulatory guidelines for adverse event reporting - Strong communication & presentation skills and is a strong standout colleague Physical Requirements / Work Environment:
PPD values the health and wellbeing of our employees.
We support and encourage individuals to build 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.
- Able to work in non-traditional work environments.
- Able to use and learn standard office equipment and technology with proficiency.
- Able to perform optimally under pressure while prioritizing and balancing multiple projects or activities.
- May have exposure to potentially hazardous elements typically found in healthcare or laboratory environments.
- This role requires independent travel up to 5%, inclusive of traveling in automobiles, airplanes, and trains.
The salary range estimated for this position is $220,000 - $280,000.
This position will also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy.
Actual compensation will be confirmed in writing at the time of offer.
We offer a comprehensive Total Rewards package that our US colleagues and their families can count on, which generally includes:
- A choice of national medical and dental plans, and a national vision plan - A wellness program, andvaluable health incentive opportunities for company contributions to a Health Reimbursement Account (HRA) or Health Savings Account (HSA) - Tax-advantaged savings and spending accounts and commuter benefits - Employee assistance program - Paid Time Off, 10 paid holidays annually, 8 hours of volunteer time, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, short- and long-term disability, and volunteer time off in accordance with company policy - Retirement and savings programs, such as our competitive 401(k) U.
S.
retirement savings plan 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 at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
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.
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.
Job SummaryJob number:
R-229812Date posted :
2023-05-12Profession:
Clinical ResearchEmployment type:
Full time.
Estimated Salary: $20 to $28 per hour based on qualifications.
Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer.
We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Due to continued growth, CRG is now looking to appoint an Associate Medical Director/Medical Director of Pulmonary/Critical Care, to join our team of Medical Directors in North America.
This role can be office-based or home based.
The Associate Medical Director/Medical Director will be responsible for providing medical support and medical advice for clinical trials and safety evaluation within the PPD Pharmacovigilance department.
A day in the Life:
- Provide study, project and program-specific medical monitoring and review services, including but not restricted to:
- Leading of all medical aspects of contracted tasks.
Supervising of safety variables.
- Discussing with clients, investigators and healthcare professionals of medical issues in the pre and post approval services by using accurate medical judgment, interpretation and decision.
- Provide medical consultation to team members and answer study related medical questions.
Communicate clearly with associates and clients, maintaining and open line of communication to ensure all procedures are followed appropriately - Analysis and assessment of safety data to identify and run emerging safety signals.
- Medical review of individual case safety reports, serious adverse event reports and clinical outcome reports.
- Assist in Business Development activities - Present PPD standard medical safety processes to clients at business development meetingsand connect with various medical communities to explore and expand PPD business.
- Participate in training of project teams.
- Provide therapeutic and protocol training as needed.
- Write, review and approve reports, regulatory submissions and protocols, ensuring that the medical content is accurate and complete.
Keys to Success:
Education - MD, MB/BS or equivalent degree and strong medical knowledge, validated clinical experience handling Pulmonary/Critical Care patients in hospital practice - Significant experience within pharmaceutical industry, clinical trials or pharmaceutical medicine is beneficial - Is proficient in spoken and written English - Solid understanding of regulatory guidelines for adverse event reporting - Strong communication & presentation skills and is a strong standout colleague Physical Requirements / Work Environment:
PPD values the health and wellbeing of our employees.
We support and encourage individuals to build 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.
- Able to work in non-traditional work environments.
- Able to use and learn standard office equipment and technology with proficiency.
- Able to perform optimally under pressure while prioritizing and balancing multiple projects or activities.
- May have exposure to potentially hazardous elements typically found in healthcare or laboratory environments.
- This role requires independent travel up to 5%, inclusive of traveling in automobiles, airplanes, and trains.
The salary range estimated for this position is $220,000 - $280,000.
This position will also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy.
Actual compensation will be confirmed in writing at the time of offer.
We offer a comprehensive Total Rewards package that our US colleagues and their families can count on, which generally includes:
- A choice of national medical and dental plans, and a national vision plan - A wellness program, andvaluable health incentive opportunities for company contributions to a Health Reimbursement Account (HRA) or Health Savings Account (HSA) - Tax-advantaged savings and spending accounts and commuter benefits - Employee assistance program - Paid Time Off, 10 paid holidays annually, 8 hours of volunteer time, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, short- and long-term disability, and volunteer time off in accordance with company policy - Retirement and savings programs, such as our competitive 401(k) U.
S.
retirement savings plan 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 at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
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.
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.
Job SummaryJob number:
R-229812Date posted :
2023-05-12Profession:
Clinical ResearchEmployment type:
Full time.
Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
