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Associate Director Medical Information Jobs

Associate Director, Melanoma Medical Communications
By Bristol Myers Squibb At ,
Working knowledge of Microsoft suite of applications, and familiar with publication management tool (DataVision)
Ability to manage timelines and quality of work using strong leadership, organizational, communication, facilitation, and interpersonal skills
A minimum of 4 years of pharmaceutical/healthcare industry experience with a focus on medical communications; experience in Oncology is preferred
Strong scientific knowledge of therapeutic and disease research areas, including HEOR, and familiarity with drug development and product lifecycle
Experience leading and executing across cross-functional, cross-cultural project teams, and collaborating across a stakeholder matrix, multiple markets, and global geographies
Outstanding interpersonal, written, and verbal communication skills
Associate Director, Medical Information
By Alkermes, Inc. At , Waltham

The Associate Director, Medical Information will assist in the strategic and operational oversight Medical Information related to Alkermes product and participate in the medical review and approval ...

Hsp Associate Medical Director
By Amedisys At , Media, 19063, Pa
A full benefits package (with affordable health insurance options).
Fleet vehicle program (for full-time caregivers meeting certain requirements).
Board certification in hospice and palliative care preferred.
Enjoy great perks and benefits
Up to $500 in wellness rewards and up to $1,200 in free healthcare services paid for by Amedisys yearly.
Infertility coverage, adoption reimbursement and paid parental leave.
Medical Information Manager Jobs
By Randstad Life Sciences US At Greater Chicago Area, United States
Excellent project management and organizational skills with the ability to prioritize and multitask
We are looking for professionals with these required qualifications and skills to achieve our goals:
Customer-focus, problem solving abilities and strong conflict resolution skills
Proficiency in Medical Information Customer Relationship Management (CRM) systems and cloud-based content management systems (e.g., SharePoint, Veeva)
Collaborate with groups outside MA (Medical Information global, Patient Experience, Legal, Commercial, Compliance, etc.) as appropriate
Verify Medical Information Request Forms (MIRFs) from the field sales force are unsolicited per applicable country requirements
Director, Medical Information Jobs
By bluebird bio At United States
Demonstrated experience in Medical/Drug information communication and management with a customer focus as well as continuous improvement of processes/assets
Excellent oral and written communication skills and interpersonal skills
Experience leading projects and teams
Gene Therapy, rare disease experience and new product launch experience preferred
Apply scientific expertise consistent with the regulatory/compliance landscape to deliver high quality medical information
Work cross functionally with the broader organization to develop/update SRDs
Medical Information Specialist Jobs
By Revance At Nashville, TN, United States
Experience using Customer Relationship Management (CRM )systems
Document the medical inquiries and fulfillment accurately within the Customer Relationship Management (CRM) system
Excellent communication skills, both written and oral
Working knowledge of drug development, regulatory approval processes, clinical trial methodologies, and guidelines
Team oriented with excellent interpersonal skills and ability to develop and maintain effective professional relationships
1-3 years of medical information or medical affairs experience in a life science, pharmaceutical, or medical device company
Medical Information Coordinator Jobs
By EVERSANA At Emeryville, CA, United States
MINIMUM KNOWLEDGE, SKILLS AND ABILITIES:
Maintain product, therapeutic area, and client specific requirements knowledge.
Hours: Able to work full time and be flexible with work scheduling as required by clients and management.
Experience and/or Training: Strong clinical background and excellent verbal/written communications skills. Strong healthcare background and excellent verbal/written communications skills.
Utilize writing skills for adverse event and product complaint narrative during intake as well as documentation of medical inquiry.
On-call responsibilities on an as assigned basis.
Medical Information Coordinator Jobs
By EVERSANA At San Francisco, CA, United States
Maintain product, therapeutic area, and client specific requirements knowledge.
Hours: Able to work full time and be flexible with work scheduling as required by clients and management.
Experience and/or Training: Strong clinical background and excellent verbal/written communications skills. Strong healthcare background and excellent verbal/written communications skills.
Utilize writing skills for adverse event and product complaint narrative during intake as well as documentation of medical inquiry.
On-call responsibilities on an as assigned basis.
Education: Life sciences degree, post-secondary education in healthcare-related field or equivalent healthcare credentials.­
Associate Medical Director Jobs
By CommuniCare Health Services At Cincinnati, OH, United States
Conduct prior authorization and utilization management activities including adverse determinations.
Provider network accessibility, availability and qualifications]
Assure adherence to documentation and requirements as set forth in the Model of Care for each MA SNP plan
Requires at least 15 years of Clinical Experience.
Experience in working in post-acute facilities, assisted living facilities, home and community-based service settings preferred.
Geriatric training and experience preferred but not required.
Associate Medical Director, Neuroscience Development
By BioSpace At North Chicago, IL, United States
Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred.
Must possess excellent oral and written English communication skills.
Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research.
Ability to run a clinical research study with appropriate supervision.
Strong desire to collaborate in a cross-functional setting.
Ability to interact externally and internally to support global scientific and business strategy.
Associate Medical Director/Scientific Director - Global Medical Affairs - Immunology
By BioSpace At North Chicago, IL, United States
Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in the design of protocols preferred.
May assist in the development of scientifically accurate marketing materials, medical education programs, advisories, and symposia.
Minimal clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent.
1-2 years of experience is preferred.
Ability to interact externally and internally to support global business strategy. Must possess excellent oral and written English communication skills.
May assist with the scientific review, development, execution and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities.
Medical Information Specialist Jobs
By Mindlance At Princeton, NJ, United States
The Medical Information Contractor’s responsibilities will include the following:
• Limits corporate liability by meeting the medical ethical and legal responsibilities of providing product/device related information
• Serves as an educational resource to both internal and external customers
• 1-3 years’ experience with providing medical information to customers
• Excellent interpersonal, communication and negotiation skills.
• MS Office; Experience with MI Systems a plus, but not required
Associate Director, Medical Writing
By Arcus Biosciences At , Remote $165,000 - $185,000 a year
Experience with electronic document management systems (e.g., Veeva Vault).
In-depth knowledge of industry regulations, guidance, and regulatory documentation requirements including thorough knowledge of ICH guidelines.
In conjunction with the Head of MW, defines and manages MW and QC resource needs and effectively communicates with cross-functional teams.
Excellent verbal communication and technical writing skills including tact and diplomacy in dealing with complex projects and teams.
Experience interacting and communicating timeline expectations with cross functional study team members.
Ensures appropriate communication on project and program-related matters with the Head of MW.
Associate Director, Medical Information Content
By Moderna Therapeutics At , Cambridge, 02139, Ma
Vacation, sick time and holidays
Volunteer time to participate within your community
Paid sabbatical after 5 years; every 3 years thereafter
Generous paid time off, including:
Associate Director/Director - Medical Communications Lead
By AnHeart Therapeutics At United States
4+ years of related experience at a pharmaceutical company or a medical communications agency
ØExperience managing budgets and vendor partnerships.
ØPartner with medical directors on development of medical strategy and planning, insight collection initiatives, and publications.
ØPartner with external stakeholders such as key opinion leaders, investigators, collaborators, and vendors for medical communication activities.
ØLead and establish internal scientific training, medical information, expanded access, and grant review infrastructure as needed.
ØEnsure medical communication projects remain on strategy, within budget, and are executed promptly.
Associate Director, Medical Information
By LEXICON PHARMACEUTICALS At , The Woodlands, 77381, Tx
Minimum of three years of related work experience in the biopharmaceutical industry including understanding of the regulatory environment
Cardiometabolic, heart failure, and/or renal biology experience is highly preferred
Demonstrated ability to lead initiatives, manage projects and work cross-functionally with a highly ethical/compliant/results driven/customer service orientation
Strong skills with literature searches, interpretation and verbal/written communication of complex medical, pharmacological, and scientific data to a variety of audiences
Excellent verbal and written communication skills coupled with strong interpersonal/team skills
Doctorate level degree (PharmD, MD, PhD) in life sciences/medical field
Senior Manager, Medical Information
By Apellis Pharmaceuticals At , Remote
Collaborates with internal stakeholders for pre- and post-approval product/indication launches and supports the life cycle management of products
Assist with Call Center management, including on-going training and coaching to provide excellent customer service
Exceptionally strong writing, communication, and interpersonal skills
Knowledge of medical publication searching and literature review
Conducts prompt execution on researching and writing custom responses for escalated medical inquiries
Analyze reports and metrics from the MI documentation database for trends and insights
Associate Medical Director, Pulmonary Medicine
By Parexel At , Remote
Excellent verbal and written medical communication skills
Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
Applicants should demonstrate certain skills to be successful in the candidate process:
Provision of medical expertise and leadership to Parexel teams during client bid pursuit meetings
Consultancy on protocol development or drug development programs
Perform review of medical and study related documents for medical accuracy, completeness and clarity
Associate Director/Director, Medical Writing
By FibroGen, Inc. At , Remote $223,200 - $238,200 a year
Serve as submission lead for complex regulatory submissions, with responsibilities including development and management of document timelines.
Manage or supervise less experienced writers and contractors to ensure the highest quality of medical writing and adherence to document standards.
Expertise with regulatory document management systems (e.g. Veeva).
Coaches, trains, and provides guidance to less experienced writers or contractors.
Experience in providing oversight of third party vendor contracts to ensure on-time and on-budget delivery.
Demonstrated experience in effective collaboration with multiple stakeholders both internally and externally including vendor partners, FDA and other Health Authorities.
Associate Director, Medical Information Novartis
By Novartis At , East Hanover, 07936, Nj $158,400 - $237,600 a year
Responsible for Project management related to TA or department initiatives
Understanding of processes and definitions of roles and responsibilities within TAs
PharmD, MD or healthcare-related PhD (Bachelor degree in pharmacy with significant industry based medical information experience also acceptable)
Pharmaceutical Industry Experience; minimum 2-3 years in MIM role or equivalent Medical Information experience
Excellent verbal and written communication skills
Business knowledge and commercial marketing understanding