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We got a new job details in Parexel – USA & they are Hiring Candidates for Medical Director – Cardiology
Company Name : Parexel – USA
Company Location : United States
Job Position : Medical Director – Cardiology
Job Category : Jobs in United States
Job Description :
Bring your Cardiology expertise to an Industry Leader, Parexel!
This is a fantastic opportunity to join Parexel’s highly recognized Medical Sciences Team as we continue to grow our incredibly dedicated and talent Medical Sciences Team!
As a Medical Director, you will work closely with some of the best and brightest in the industry and assist our clients in the journey of getting new and innovative drug treatments into the hands of those who need them most. You will be a member of a fantastic and cohesive global team with great mentors and work with small to large clients across a broad spectrum of diseases.
Overall responsibilities of the Medical Director are to:
Provide medical and safety monitoring for assigned projects
Provide medical expertise and leadership to support business development and pre-award activities
Medical Support / Medical Monitoring for projects and studies contracted to Parexel
Deliver all medical support required for successful delivery of the projects according to contracted agreement with the sponsor (i.e.: tasks and time per task contracted) and according to the assigned role (Global Lead Physician GLP or Regional Lead Physician RLP)
Medical support includes but is not limited to the following:
Participate actively in study planning with feasibility leaders, solution consultants
Participate in team project and investigator meetings
Provide training of study teams on TA indication and protocol Note that this does not include any direct medical advice on patient care or management
Communicate with relevant sponsor counterparts on challenges and accomplishments related to assigned project/study
Participate in the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated clinical and statistical summary reports, safety plans, Informed Consent Forms, etc. in conjunction w/ clients/sponsors or in conjunction with other Parexel departments
Deliver medical monitoring activities according to MMP during the study conduct:
Answer to site/study team questions relating to the study conduct or protocol
Review and sign off all data listings / tables, protocol deviations, datasets, for medical accuracy/consistency in accordance with study plans (Medical Monitoring Plan, Medical Data Review Plan, Data Surveillance Plan etc.)
Deliver medical leadership to the project in close coordination with the Project Leader according to the role assigned either GLP or RLP by
Timely identifying risks and challenges
Pro-actively proposing and/or delivering relevant actions contributing to the success of the study/project and risk mitigation
Creating a sense of urgency on any matters pertaining to safety of study participants and scientific integrity of the study
Attend and support any audits or inspections pertaining to assigned studies even if not directly involved in the audited activities
Participate in periodic rotas including night and weekend shifts e.g. for emergency medical contact and emergency unblinding phone requests for Parexel studies, as applicable and/or appropriate for the MD
Provide risk assessment of clinical trials for local sponsorship as needed with the support of the designated Senior Medical Director/ Global Head of TA (as appropriate)
Provide medical input into PV workflows and projects and participate in safety processing for studies including medical review of serious adverse events
Support regulatory safety reporting activities
Ensure client needs and concerns are addressed to ensure customer satisfaction
Actively listen to, solicit and address client feedback and suggestions regarding medical study-related activities in order to enhance client satisfaction
Follow up sponsor satisfaction metrics pertaining to medical activities in assigned studies and propose /execute remediation plan in coordination with line manager and Project Leader in case of client dissatisfaction
Business Development Support
Support Business Development, as agreed with Line Manager, while adequately balancing time devoted to this activity with billable tasks
In line with business development objectives, meet and attend phone conferences with clients to communicate and detail Parexel medical expertise and experience in a therapeutic area or in an indication
Provide medical expertise/ leadership in Proposal Development Teams (PDTs) for client bid pursuit meetings
Attend preparation meeting and Bid pursuit meetings as required
Provide support for marketing activities as requested.
Share sponsor insights and experiences (strategy, history, culture, priorities etc.) with peer and proposal teams
Provide medical expertise to client as contracted across multiple channels and interactions such as:
Consultancy on protocol development, drug development program etc.
Medical review of various documents which might be audited by clients and regulatory agencies
More generally in any client interactions
Provide medical expertise and training to other Parexel personnel, as required.
As appropriate write clear, concise medical documents
Participate in activities to raise, coordinate and promote Parexel medical expertise both internally and externally including but not limited to internal therapeutic area meetings, trainings, white papers, slide sets, publications etc.
Experience in clinical medicine (general or specialist qualifications) with a specialty in a “therapeutic area” which is expected to be kept up to date
Experience leading, mentoring and managing individuals/ a team, preferred, but not essential
A background in clinical aspects of drug development, including all aspects of Medical Monitoring and study design/execution, preferred
Good knowledge of the drug development process including drug safety, preferred
Excellent interpersonal skills including the ability to interact well with sponsor/client counterparts
Excellent time management skills
Client-focused approach to work
Successful applicants will be:
Medically qualified in an acknowledged medical school with completion of applicable clinical training (residency, internship, fellowship)
Board certified/Board eligible in Cardiology with extensive clinical experience
Experience as a Physician in Industry or as a clinical trial investigator is a plus.
The ability to travel 15-20% may be required in the future.
Employment is contingent on disclosure of your COVID-19 vaccination status and, if relevant, proof of vaccination.
Why Work at Parexel
There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. What if you had a partner to support you as you reach the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner who is dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?
That’s Parexel. We’re a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we bring to our clients and the opportunities we bring to our team get better with every step.
How can we help you on your journey? Find your path, and learn more on LinkedIn , YouTube , Facebook , Twitter , and Glassdoor .
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