Clinical Research Physician Resume Sample
Loraine Wyman
2142 Trever Glen,
Philadelphia,
PA
+1 (555) 545 7259
Work Experience
Medical Director, Clinical Research Physician
01/2016
-
PRESENT
Chicago, IL
- Support the development and implementation of the medical affairs launch strategy, including responsibility for ensuring that the needs and education of payers, prescribers, and the other nonregulatory stakeholders who influence patients' treatment access or benefits are met. Key activities include
- Staff coordination is required at the USAMRIID level and with other coordinating services or agencies
- The physician shall have a state medical licensure within the U.S. or U.S. territories
- Complete all Government training required for position and/or organization
- Provide protocol, Risk management plan & disease training as appropriate at Investigator’s Meetings or scientific venues or internally
- Very good medical knowledge in at least one of the disease areas under investigation, trial related risks, study designs and their potential impact on patient's wellbeing and validity of the trial
- Very good knowledge of operational tasks and basic knowledge of the regulatory landscape for clinical research, especially GCP, Declaration of Helsinki, German, European and US drug laws
- Delivery of high quality solutions under high time pressure requires prioritization and time management skills and characterizes your way of working
Clinical Research Physician
04/2011
-
12/2015
San Francisco, CA
- Fluency in written and spoken English and German is required
- Contribute to the development of the overall strategy and clinical plan for development of clinical compounds, focusing on studies required for product decision or regulatory submission. Support preparation of high-level plan for phase 2 and 3 studies for early phase and/or detailed biopharm plan to support submission
- Collaborate with other functional areas (Global Patient Safety, PK/PD, ADME, Statistics, Tailored Therapeutics organization) in the development of methods for assessing special clinical safety pharmacology studies (e.g. TOT studies)
- Collaborate with other quantitative scientists (e.g., PK/PD, statistics, molecular epidemiology, ADME, modeling and simulations) to integrate study development and conduct with disease-progression and drug disease response models
- Contribute, as an integral member of the Clinical Pharmacology team, to global alignment of Phase I and II clinical studies as well as submission planning activities
- Work with Brand Team/Business Unit colleagues to provide appropriate market differentiation and regulatory support in the biopharm submission plan
- Communicate and collaborate with Sr. Medical Director to ensure life cycle plans for drugs in development address customer needs or communicate to Global Development teams, Global Health Outcomes (GHO), PRA, Therapeutic Area Program Phase, and Early Phase /EPM /Translational Medicine teams
Clinical Research Physician, Diabetes
12/2005
-
10/2010
Los Angeles, CA
- Communicate local/regional research needs and collaborate with other regions and the Global Development team, GHO, and PRA teams to ensure Phase 3, 3b, and 4 clinical programs meet the needs of local/regional customers
- Understand and remain updated with the pre-clinical and clinical data relevant to the molecule
- Represent the clinical needs of the country/region to the business unit medical leadership in the development of clinical strategies, development plans and study protocol design
- A board certified physician
- Currently licensed within the State of Maryland
- Related research experience in the areas of tobacco, substance use/abuse, health behaviors or clinical science
- Medical/health experience in a hospital or clinic setting following completion of a residency program
- Experience ensuring high-quality, on-time deliverables in a fast-based environment
- Provide input into clinical sections of IND’s, Investigator Brochures, CTA’s , ISS’, ISE’s and clinical expert reports
Education
University of Illinois at Chicago
2000 - 2004
School's Degree in Clinical Medicine
Professional Skills
- Demonstrated strong communication,interpersonal,organizational,teamwork and negotiation skills
- Excellent teamwork skills, including working with those from different backgrounds
- Exceptional interpersonal skills with demonstrated successful team participation
- ≥1 years industry clinical research experience, or ≥2 years industry medical affairs physician experience
- Reguires high level of communication skills, verbal, written and presentation
- Experience in clinical research including designing and conducting clinical studies
- Experience working on projects in a matrix environment, coordinating activities and adhering to tight timelines required
How to write Clinical Research Physician Resume
Clinical Research Physician role is responsible for drug, interpersonal, software, medical, health, leadership, modeling, training, database, oncology.
To write great resume for clinical research physician job, your resume must include:
- Your contact information
- Work experience
- Education
- Skill listing
Contact Information For Clinical Research Physician Resume
The section contact information is important in your clinical research physician resume. The recruiter has to be able to contact you ASAP if they like to offer you the job. This is why you need to provide your:
- First and last name
- Telephone number
Work Experience in Your Clinical Research Physician Resume
The section work experience is an essential part of your clinical research physician resume. It’s the one thing the recruiter really cares about and pays the most attention to.
This section, however, is not just a list of your previous clinical research physician responsibilities. It's meant to present you as a wholesome candidate by showcasing your relevant accomplishments and should be tailored specifically to the particular clinical research physician position you're applying to.
The work experience section should be the detailed summary of your latest 3 or 4 positions.
Representative Clinical Research Physician resume experience can include:
- Cultivate and nurture strong collaborations, relationships and support with Investigators, Academic partners and KOL’s
- Experience in pulmonary and/or cardiovascular disease areas
- Computer literate with experience in Microsoft Software suite and other relevant packages
- Demonstrated knowledge of device/drug development process
- Experience desirable in health policy, health outcomes, statistics, payers, and/or healthcare organizations
- Excellent track record in personal engagement and leadership
Education on a Clinical Research Physician Resume
Make sure to make education a priority on your clinical research physician resume. If you’ve been working for a few years and have a few solid positions to show, put your education after your clinical research physician experience. For example, if you have a Ph.D in Neuroscience and a Master's in the same sphere, just list your Ph.D. Besides the doctorate, Master’s degrees go next, followed by Bachelor’s and finally, Associate’s degree.
Additional details to include:
- School you graduated from
- Major/ minor
- Year of graduation
- Location of school
These are the four additional pieces of information you should mention when listing your education on your resume.
Professional Skills in Clinical Research Physician Resume
When listing skills on your clinical research physician resume, remember always to be honest about your level of ability. Include the Skills section after experience.
Present the most important skills in your resume, there's a list of typical clinical research physician skills:
- Lead the development of a significant clinical development budget and effectively manage resources, funding and expenses across assigned programs
- Strong ability to work collaboratively and to respect other working cultures, including academic partners
- Good working knowledge of international regulations relating to clinical trials
- Demonstrated ability to influence others (both cross-functionally and within the function)in order to create a positive working environment
- Experience in drug development, preferably including OTC
- Clinical research or development experience in a clinical setting or a pharmaceutical/biotech industry
List of Typical Experience For a Clinical Research Physician Resume
1
Experience For Medical Director, Clinical Research Physician Resume
- Demonstrated leadership qualities with particular focus on collaborative working skills, trust and openness, irrespective of cultural setting
- Phase IIb - IV experience important
- Assists with training and provides medical input for clinical research personnel
- Travel nationally and internationally as required (estimated 20% depending on trial activity, corporate needs, etc.)
- Develop an integrated plan of action including milestones and endpoints and ensure executional excellence
- Liaise with Sponsors regarding medical issues and medical consultation
- Assist senior medical management in ensuring departmental revenue and margin targets are met
- Is responsible for driving decisions within Study Team (ST) remits together with other ST members
- Is accountable for the medical and ethical components of studies including patient safety on a study level in compliance with GCP
2
Experience For Senior Clinical Research Physician Resume
- An understanding of pharmaceutical industry R&D, particularly of major clinical milestones and of the factors which influence Drug development
- An understanding of the interplay between clinical, commercial objectives, drug safety and regulatory requirements
- Accountable for safety, scientific integrity, medico legal and medical governance aspects of assigned clinical studies
- Supports Standard Operating Procedures (SOPs), Good Clinical Practices, and all work processes to ensure the efficient and compliant clinical operation of the CRU
- Assists with the medical and clinical oversight of all aspects of function and work associated with the CRU
- Assists as necessary with IRB submissions
- Knowledge of FDA regulated drug development process is helpful. Excellent interpersonal skills; detail oriented, with ability to work in a fast-paced environment. Clinical practice experience of at least two years and board
- Collaborate with Clinical and Biostatistics/Data Management teams on review of safety data, enrolment eligibility, etc
- Provide monthly reviews of protocol deviations and AE trends
3
Experience For Clinical Research Physician, Immuno Resume
- Attend and present clinical data at internal/external meetings as needed
- Present clinical study updates as needed
- Respond to sites and address questions about assigned clinical protocols
- MBBS, M.D., D.O. or equivalent
- Establish, communicate and drive a vision and strategy for the therapy area/product
- Oversee quality, coordination and on time delivery of clinical sections of IND’s, Investigator Brochures, CTA’s , ISS’, ISE’s and clinical expert reports
- Be viewed as a global leader with the therapeutic area/disease state and considered a scientific contributor and innovator within internal and external spheres of influence
4
Experience For Clinical Research Physician Neuroscience Resume
- Lead the development of the clinical strategic plan for program/therapy area. Identify what is needed to drive the program/therapy area and the specific operational plan to get there
- Manages, forecasts, and allocates resources for the clinical program with support from Therapeutic Area Head (TAH). Accountable for timely execution of clinical deliverables within approved budget
- Member of the Clinical R&D extended leadership team
- Ensures career development of functional reports (Medical Directors) through active participation in the performance management and talent planning processes. Provides on-boarding, training, and mentoring support and contributes to the performance evaluation of team members as appropriate
- Attracts and develops talent, coaches and mentors others to higher levels of performance. Creates an atmosphere of innovation and continual improvement
- The ability to establish, communicate and drive a vision and strategy for the therapy area/program and develop and integrated plan of action including milestones and endpoints and ensure executional excellence
5
Experience For Clinical Research Physician, Diabetes Resume
- Medical experience
- Contribute to business unit and global alignment of clinical strategy and clinical plans
- Understand and keep updated with the pre-clinical and clinical data relevant to the molecule
- Communicate and collaborate with Sr. Director-Medical, Regional CRP, etc as needed.) to ensure life cycle plans for drugs in development address customer needs or communicate and collaborate such needs to global Development teams, Global Health Outcomes (GHO), PRA, Therapeutic Area Program Phase, and Early Phase /EPM /Translational Medicine teams
- Communicate local/regional research needs and collaborate with other regions and the global Development team, GHO, and PRA teams to ensure Phase 3, 3b, and 4 clinical programs meet the needs of
- Collaborate with clinical research staff in the design, conduct and reporting of local clinical trials (for example, sample size, patient commitment, timelines, grants, and governance review interactions)
- Review and approve risk profiles to ensure to ensure appropriate communication of risk to study subjects
- Participate in investigator identification and selection, in conjunction with clinical teams
6
Experience For Clinical Research Physician, Medical Affairs Resume
- Ensure that operational team has documented the completion of administrative requirements for study initiation and conduct (for example, ethical review board, informed consent, regulatory approval/notification) consistent with Good Clinical Practices (GCPs) and local laws and requirements
- Assist in planning process and participate in study start-up meetings and other activities to provide the appropriate training and information to investigators and site personnel
- Serve as resource to clinical operations personnel/ clinical research monitors, investigators and ethical review boards to address any questions or clarify issues arising during the conduct of study
- Understand and actively address the scientific information needs of all investigators and personnel
- Monitor patient safety during the conduct of studies and conduct the appropriate tracking and follow-up of adverse events, in alignment with corporate patient safety policies and procedures
- Related research experience in clinical science
- Review IIT proposals and publications, as requested by Director-Medical
- In addition, the CRP is responsible for assuring that his/her activities are clearly aligned with the strategic priorities of the respective business unit global Medical Affairs team, brand team(s), global Development team, Therapeutic Area Program Phase, Early Phase / Clinical Pharmacology, and Translational Medicine team(s)
- The Clinical Research Physician serves as a scientific resource for study teams, departments, and others as needed
7
Experience For Temp / Clinical Research Physician Resume
- Understand and anticipate the scientific information needs of payers, patients, health care providers
- Actively address payer, patient and health care providers questions in a timely fashion by leading data analyses and new clinical or health outcomes research efforts
- Contribute to the development of medical strategies to support brand commercialization activities by working closely with the global Medical Affairs and brand teams, Global Patient Outcomes/Real World Evidence and global PRA, clinical management or personnel and other cross-functional management during the development of the local business plan
- Contribute actively on an ongoing basis to the strategic planning for currently marketed brands
- Become familiar with market archetypes and potential influence on the medical interventions for the product
- Development and execution of thought leader/key influencer strategy
- Planning, development and execution of Phase 3 and 3B through Phase 4 clinical research, RWE trials, ensuring the clinical program includes a robust holistic evidence package
8
Experience For Clinical Research Physician Resume
- Medical and disease state education, publications, medical information, and medical affairs advisory boards
- Collaborate with GBD and affiliate/regional brand teams for launch preparation and serve as the primary medical leader for commercial-related activities, providing input for the following brand development activities
- Commercialization activities and program development (customer council,brand planning, etc)
- Foundational insights for patients, providers, and payers (patient segmentation, patient journey, environmental evolution, etc)
- Support priority product launches in the US, Japan, China and EU, and other key International Business Unit (IBU) countries. Serve as a resource and advocate for affiliates and regional medical affairs teams. Relay their needs back to the global team (including alliances)
9
Experience For Medical Director, Clinical Research Physician Resume
- Responsible for identifying, understanding, and engaging key thought leaders
- Oversee and provide consultation for lab report review, CRF safety review, and potential endpoint reporting, for clinical projects
- As appropriate, identify and collaborate with external scientific experts and thought leaders who share our mission and an interest in our work
- Interact with Advocacy and Professional Relations and maintain relationships with advocacy groups and professional societies
- Be aware of and ensure that medical affairs activities are "in compliance with Good Clinical Practices (GCPs), company standards, Lilly policies and procedures, company integrity agreements as applicable, and the Principles of Medical Research, and that activities are aligned with the medical vision
- Significant experience in the pharmaceutical industry in drug safety related roles
- Review & assessment of study safety data tables, listings and figures and safety sections of clinical study reports
10
Experience For Senior Clinical Research Physician Resume
- Assessment and review of integrated safety summary documents and risk management documents
- Education – MD, PharmD and/or PhD is required
- Serve as medical team leader on assigned projects
- Ensure provision of all contracted activities and identification of out of scope activities on projects assigned
- Provide medical oversight for serious adverse event reporting and tracking, and communication of safety issues to ICON staff, sponsors, and regulatory authorities
- Coordinate and provide medical training including indication training, protocol training, safety presentations for ICON clinical staff, project teams, or during investigator meetings
- Review and approve protocols, case report forms, informed consent forms (when applicable), and other miscellaneous study documentation
- Coordinate review and approval of serious adverse event narratives
List of Typical Skills For a Clinical Research Physician Resume
1
Skills For Medical Director, Clinical Research Physician Resume
- Good presentation skills. Can communicate effectively with internal and external collaborators
- Interpersonal,organizational,and negotiation skills
- Strong understanding of Oncology therapeutic area – pathology, pathophysiology, unmet needs, and treatment standards
- Experience in conducting clinical studies as medical monitor
- Medical advisor or project leader experience in industry
- ≥2 years hospital physician experience
- Clinical Research Physician experience in industry
2
Skills For Senior Clinical Research Physician Resume
- Experience in due diligence activities
- Proven ability to interpret, discuss and represent efficacy and safety data in the as-signed therapeutic area
- A scientific background with laboratory experience is desirable
- Good general medical knowledge preferably in endocrinology, cardiology or nephrology
- Experience from different organizations
- Good knowledge of biostatistics, global regulatory environment and pharmacovigilance
3
Skills For Clinical Research Physician, Immuno Resume
- Demonstrates AstraZeneca values and Behaviours
- Preferably experience in a relevant clinical research role
- Sound experience as a Clinical Research Physician, Study Physician or Medical Monitor is required
- Cultivate and nurture strong collaborations, relationships and support with Investigators, industry and academic partners and KOL’s
- Willing to relocate to Indianapolis
- Understanding of FDA regulations and GCP
- Writing and review of safety analysis (case-series review, safety topic review) to support summary documents
- Critically review documents including CRFs, Data Tables and Listings, and other reports including CSRs
4
Skills For Clinical Research Physician Neuroscience Resume
- Oversee study specific medical/safety monitoring activities, ensuring compliance with ethical, legal, and regulatory standards as well as ICON and Sponsor SOPs
- Core brand development (global positioning, global brand planning, etc)
- Involvement in clinical research or drug development in an industry environment spanning clinical activities in Phases I through IV
- Influence others (both cross-functionally and within the function) in order to craft a positive working environment
- Able to provide guidance for investigator initiated trials in cooperation with regional marketing companies
- Understand and present data at internal and external meetings, including Investigators’ meetings and Data Review Meetings
- Participates in the review and coding of adverse events and concomitant medications for accuracy and consistency
- Deep understanding of GCP, regulatory requirements and data privacy laws
5
Skills For Clinical Research Physician, Diabetes Resume
- Authors safety sections of Informed Consent documents, and assists in obtaining the consent from study volunteers
- Design, implement and manage safety monitoring plans
- Author medical/clinical reports (including CSRs) for assigned clinical programs
- PK/PD, Modeling & Simulation, ADME, Toxicology
- Provide medical/scientific consultation and therapeutic expertise including QPPV (EU)
- Liaises with relevant Pfizer sites regarding the design, conduct and progression of studies conducted at the Clinical Research Unit
- Engage and inspire the program/clinical development teams through communicating the strategic vision and the operational plan to achieve the vision
- By offering scientific and creative input, contribute to the development, review, and approval of promotional materials for the brand team
- Support training of sales representatives, and other medical representatives
6
Skills For Clinical Research Physician, Medical Affairs Resume
- Development of content to support internal training, responses to HCP unsolicited requests for information, and other medical resources
- Assist with NDA and/or MMA regulatory filing in the US & EU
- Professional association staff and leaders
- Disease advocates and lay organizations focused on relevant health issues
- Create complex strategies to develop the product and successfully articulate this to various constituents such as governance committees, project teams, clinical sub-teams, and other senior management to build enthusiasm, passion and commitment
- Demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical or biotech industry
- Excellent negotiation and diplomatic skills, experience with health authorities required
7
Skills For Temp / Clinical Research Physician Resume
- Excellent leadership, management, interpersonal, communication, and problem solving skills
- Considerable organizational awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams
- In-depth Medical/scientific and operational expertise in hematology/oncology. Demonstrated technical knowledge and innovation in clinical development study designs that provide relevant evidence to decision-makers
- ≥2 years hospital physician experience, or ≥1 years industry medical experience with experience to independently take care of patients
- Demonstrates current knowledge of relevant local regulations and compliance requirements and communicates to global teams as required
8
Skills For Clinical Research Physician Resume
- Demonstrates knowledge of applicable SOPs, policies, procedures, and guidance documents
- Strong ethics, patient-focus, and ability to earn credibility and trust
- Applies knowledge of regulatory / industry rules to work in a local regulated environment
- Expertise to represent company as safety expert for clinical trials to external regulatory and compliance bodies such as regulatory agencies, boards of health, and ethics committees
- Experience in drug development for rheumatological diseases
- Therapeutic area directors, managers, or project managers
- Product directors, managers, and associates of the brand
- Global patient outcomes research consultants/research scientists and global patient outcomes liaisons
- Therapeutic area physicians, global brand physicians, early phase physicians, clinical research scientists, and Regional Medical Leaders, Directors-Medical
9
Skills For Medical Director, Clinical Research Physician Resume
- Corporate or regional patient safety physician(s)
- Fluent in English, both written and verbal communications
- Works directly with clinical research personnel, reviewing lab data, performing physical assessments, obtaining medical histories, and evaluating inclusion/exclusion criteria for study volunteers
- Participates in on-call and general physician coverage schedule for the CRU
- Supports the implementation and application of PIMS in the CRU
- Provides support for the preparation of clinical protocols, integrated clinical and statistical summary reports, and other documents as requested
- Liaises with local/regional medical consultants as necessary
- Participates in the review of source data and/or data listings of safety data, including adverse experiences, lab data, and vital signs data, to establish the presence or absence of abnormal trends, or if noted, follow-up as appropriate with the CRU clinical team, the CRU project team, the sponsoring Pfizer site, and regulatory agencies
10
Skills For Senior Clinical Research Physician Resume
- Participates in the review of individual adverse event reports for accuracy and clinical importance, and characterizes their relationship to the study drug, severity and seriousness
- Knowledge of clinical development process and GCP
- Knowledge of and regulatory requirements
- Board Certification in respective discipline
- Minnesota licensure in respective discipline
- Medical Doctor Speciality in Neurology, Internal Medicine or any other with established expertise in Headache and/or pain management
List of Typical Responsibilities For a Clinical Research Physician Resume
1
Responsibilities For Medical Director, Clinical Research Physician Resume
- Review and approve final study reports or other clinical documents
- Direct code-break activities (as appropriate)
- Act as QPPV (EU) as assigned
- Serve as part of the medical management team
- Supervise, develop and mentor lower level Medical Affairs and Drug Safety staff as assigned by the Regional Vice President
- Represent ICON Medical Affairs at teleconferences and meetings
- Ensure quality of medical deliverables in accordance with project plans and ICON standards
- Represent Medical Affairs in business development activities including general capabilities presentations, bid defenses, medical costing estimates, and change order assumptions
2
Responsibilities For Senior Clinical Research Physician Resume
- Provide input for monthly status reports, departmental activities, and project / performance related issues to the Director / Senior Director / Regional Vice President / Senior Vice President Medical Affairs
- Other activities as identified and requested by senior
- Interact with consultants, clinical pharmacologists, clinical investigators, and affiliate CRPs to plan, initiate, and conduct worldwide clinical trials
- Develop and/or review protocols for clinical trials
- Prepare and present documentation of clinical trial results to corporate committees, regulatory agencies, and outside audiences
3
Responsibilities For Clinical Research Physician, Immuno Resume
- Publish results of research projects
- Explore and take advantage of opportunities for extramural scientific relations
- To assess and interpret study clinical data, e.g. Pulse, BP, ECG’s, laboratory tests, adverse events etc
- Board certification in a relevant clinical specialty such as rheumatology, nephrology, clinical immunology, internal medicine, or other relevant specialty
- Medical Doctor or Doctor of Osteopathy with speciality in Neurology or Primary Care (IM, FP) (required) - OR - prior pharmaceutical industry medical affairs experience
- Therapeutic area physicians, global brand physicians, early phase physicians, and directors-medical
- Health outcomes research consultants/research scientists and health outcome liaisons
- Regulatory directors, scientists, and associates
4
Responsibilities For Clinical Research Physician Neuroscience Resume
- Product directors, managers, and associates of the brand teams
- Knowledge of clinical trial design and statistics
- Proven learning agility: comfortable with complexity and able to explain complexity in simple words. Curious, find solutions to tough problems. Can deliver results under first time conditions. Interested in continuous improvement. Self-aware and comfortable with diversity of people and opinion
- Advisors-Clinical Project Management
- Clinical research staff (CTM, CPM)
5
Responsibilities For Clinical Research Physician, Diabetes Resume
- Corporate patient safety physician
- High-level clinical and scientific knowledge of assigned therapeutic area
- General knowledge of all aspects of the drug development process
- Pfizer US/PR Exempt grade 17
- Education in Pharmaceutical Medicine
6
Responsibilities For Clinical Research Physician, Medical Affairs Resume
- Clinical research expertise in relevant therapy area in study design, protocol development, monitoring and implementing clinical trials, interpreting and reporting trial results
- Agile responsiveness to scientific data. Credible in scientific and commercial environments
- Represent Clinical Development in cross-functional and cross-divisional due diligence teams, and lead clinical due diligence activities; provide clinical development expertise and support to Business Development & Licensing
- Directly lead or oversee all aspects of medical and clinical support of assigned clinical programs and trials within the US
- Eligibility for Medical license in the US highly desirable
- Work and communicate efficiently with internal partners
- Manage multiple tasks simultaneously with attention to detail
7
Responsibilities For Temp / Clinical Research Physician Resume
- Provides strategic medical (CVMD) and scientific knowledge and support in the design, initiation, execution and completion of a clinical study
- Is accountable for study designs and study design concept delivery
- Is accountable to deliver medical information / answers to Regulators, Ethic Committees, Marketing Companies, investigators/sites, and provides clarifications as well as solves medical issues in the study team
- Is accountable to the Global Clinical Leader (GCL) or delegate for the medical aspects and designs of studies
- Is accountable for delivery of all relevant study documents (e.g Protocol, Statistical Analysis Plan, amendments, Informed consent, Case report forms, safety and risk based monitoring plans)
- Is accountable for safety surveillance on a study level including the process for Adverse Events (AE)/ Serious AE reporting - query investigator on missing/unclear data, review blinded safety data and escalate to GCL/Global Safety Physician when needed
8
Responsibilities For Clinical Research Physician Resume
- Is medically accountable for international investigator meetings, and support to Marketing Companies (MC) for national activities
- Approves (with the GCL) the Clinical Study Report; including preparation and production there of (Introduction, Results, Discussion)
- Is accountable for CST induction and education of new members in the study team, as well as others involved in the study
- Collaborates seamlessly and efficiently with global colleagues at other R&D sites
- Stays updated on scientific relevant literature, and is able to message key impactful points, as applicable
9
Responsibilities For Medical Director, Clinical Research Physician Resume
- Delivers analyses of clinical data in a balanced, statistically sound fashion, to drive interpretations and further idea generation
- Serves as a source of medical expertise for the Product Team, in analyses and interpretation of medical data
- Works with international colleagues and with external Alliance partners on development initiatives and regulatory issues
- Applies strategic intent of AstraZeneca when working with Alliance partners, Regulatory Authorities, payers, opinion leaders, prescribers and consumers of AstraZeneca products
- Scientific communication associates
- Medical information associates
- Active M.D or DO License
10
Responsibilities For Senior Clinical Research Physician Resume
- Clinical research staff
- Able to think globally, strategically and innovatively about the future of the disease state and company’s therapeutic agents and possess a solid understanding of the pharmaceutical industry, company competition and commercial side of business, including Marketing and Sales, Market Access, Pricing/Reimbursement, Business Development, Medical Affairs and Supply Chain
- Collaborate with the business unit geographical regions, Discovery, Program Phase Medicine, and Clinical Pharmacology in the development and maintenance of a Draft Launch Label and Value Proposition that addresses key customer needs (patient, provider, and payer); the product lifecycle plan, clinical strategies, development plans and study protocol design
- Through the application of scientific and medical training, clinical expertise, and relevant clinical experience, the Business Unit - Medical Affairs Clinical Research Physician (CRP) is an integral member of the medical affairs, development team for strategic planning in the support of launch and commercialization activities of molecules approved for rheumatology indications
- Collaborate with the business unit geographical regions, Discovery, Program Phase Medicine, and Clinical Pharmacology in the development and maintenance of a Draft Launch Label and Value Proposition that addresses key customer needs (patient, provider,and payer):the product lifecycle plan,clinical strategies, development plans and study protocoldesign
- Preference for post graduate training with board certification in specialty relevant to Pain Management/Therapies, e.g., Pain Management Physician, Physical Medicine & Rehabilitation (Physiatrist), Neurologist, Orthopedic Surgeon, Neurosurgeon, Anesthesiologist. - OR - post graduate training in Family Practice or Internal Medicine, preferably with fellowship training in pain treatment
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