Sr Medical Scientist - HIV - Local Studies - Portfolio Management (Support) - US - Home Based Location: Morrisville, NC, United States Job ID: 25109313-OTHLOC-1500-2DWY-2DR Job Description: Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health - We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. - We are committed to building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life. - We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities - Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). - Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical - plans. - Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. Pro-actively identifies and resolves medical data review issues as they arise. - Authors medical data queries and reviews query responses, approves query closure in association with Medical Director. - May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. - Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed. - Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review. - Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the - project leads in a timely manner. - Attends and present at Trusted Process meetings and may participate in internal and external audits. - Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology. - Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Requirements: - Degree in life sciences (Bachelors) or related discipline in natural sciences/health care field or equivalent combination of education and experience with 2-3 years of clinical research experience. - Excellent time management skills to handle multiple tasks and meet deadlines while delivering high quality work in a highly regulated and dynamic environment is essential. - A self-starter and comfortable with fluctuating timelines, work demands and changes in scope of work. - Ability to troubleshoot situations as needed and understands when issues or questions need to be escalated to the leadership. - Understanding of scientific principles to assure effective and high-quality medical data analysis. - Excellent written and oral communication skills. - Excellent computer skills: MS Office programs, spread sheets, presentations. Must have knowledge of drug development and demonstrated proficiency with ICH/GCP guidelines. - Strong team player with excellent interpersonal skills and ability to work effectively in a cross-functional team environment At  Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements. Salary Range: $79,800.00 - $139,600.00 The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Location: Morrisville United States Job Description: Description Sr Medical Scientist - HIV - Local Studies - Portfolio Management (Support) - US - Home Based Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health - We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. - We are committed to building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life. - We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities - Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). - Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical - plans. - • Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. Pro-actively identifies and resolves medical data review issues as they arise. - • Authors medical data queries and reviews query responses, approves query closure in association with Medical Director. - • May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. - • Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed. - • Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review. - • Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the - project leads in a timely manner. - • Attends and present at Trusted Process meetings and may participate in internal and external audits. - • Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology. - • Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Requirements: - Degree in life sciences (Bachelors) or related discipline in natural sciences/health care field or equivalent combination of education and experience with 2-3 years of clinical research experience. - Excellent time management skills to handle multiple tasks and meet deadlines while delivering high quality work in a highly regulated and dynamic environment is essential. - A self-starter and comfortable with fluctuating timelines, work demands and changes in scope of work. - Ability to troubleshoot situations as needed and understands when issues or questions need to be escalated to the leadership. - Understanding of scientific principles to assure effective and high-quality medical data analysis. - Excellent written and oral communication skills. - Excellent computer skills: MS Office programs, spread sheets, presentations. Must have knowledge of drug development and demonstrated proficiency with ICH/GCP guidelines. - Strong team player with excellent interpersonal skills and ability to work effectively in a cross-functional team environment At  Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements. Salary Range: $79,800.00 - $139,600.00 The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Role Description The Federal Medical Science Liaison (FedMSL) is a field-based scientific professional who represents the Medical Affairs organization with scientific and clinical leaders at federal entities such as Veteran’s Affairs and Federal Bureau of Prisons. The FedMSL works throughout a product's lifecycle, helping to ensure that company products are utilized safely and effectively, serves as a scientific resource within the medical community, establishes and maintains peer-to-peer relationships with Indian/Tribal Health, VA, criminal justice, and is a scientific expert to internal colleagues at the company. MSLs provide medical information and education through balanced scientific exchange and provide clinical and scientific support for Braeburn and the Medical Affairs department at the direction of Medical Affairs management. Specific Duties - Provide disease state awareness, product information and pharmacoeconomic analyses as presentations or other forms of scientific exchange to managed care organizations, payers, and other formulary decision makers per unsolicited requests. - Maintain comprehensive, up-to-date scientific expertise of disease state, clinical information, product data, and the competitor landscape within the relevant therapeutic area(s). - Identify and develop peer-to-peer relationships with Key Opinion Leaders (KOLs) and major federal stakeholders by engaging in ongoing and balanced scientific exchanges in disease areas of strategic importance to Braeburn. - Present scientific product-related data and disease awareness information in the federal, hospital, institutional, and academic settings. - Serve as liaison between healthcare professionals and Braeburn for unsolicited Investigator-Initiated Trials (IITs). - Address unsolicited requests for medical information from healthcare professionals via written and verbal responses, with appropriate documentation. - Support Company sponsored trials and other research initiatives including clinical trial site recruitment as needed. - Support external healthcare professional Speaker Training and provide Advisory Board support as needed. - Present information for initial and ongoing training of internal and external partners pertaining to disease state, product and competitive landscape information. - Provide medical booth and session coverage at scientific/medical meetings. - Align day-to-day activities with Medical Affairs strategic objectives, with flexibility depending upon evolving business needs. - Proactively and collegially interact with other field-based and internal colleagues; provide information to internal colleagues regarding regional and local issues that impact business and/or healthcare practice. - Always comply with company and compliance policies, and internal and external guidelines. - Support internal Medical Affairs projects as requested. Qualifications - Relationship building skills with top tier medical experts. - Possesses business and scientific acumen demonstrated by communication of complex scientific and clinical information to colleagues, academicians, and healthcare decision makers. - Understanding of the managed care arena and the application of pharmacoeconomic principles is desirable. - Teamwork, leadership, timely decision making and results orientation skills in meeting business objectives. - Strong interpersonal, organizational, team, written and verbal communication and presentation skills. - Strong work ethic and commitment to excellence. - Ability to thrive in a virtual environment. - Candidate must hold a valid driver’s license and be able to travel up to 60–70%. Requirements - The qualified candidate will have an advanced degree in a health-sciences related field such as a PharmD, MD, DO, PhD. - 5+ previous MSL or relevant pharmaceutical industry experience preferred. - Experience in addiction medicine preferred. - Experience in federal and state medicine preferred. Company Description Braeburn is dedicated to delivering solutions for people living with the serious consequences of opioid use disorder. At Braeburn, we challenge the status quo and champion transformation of the management of opioid use disorder (OUD) by partnering with the community to create a world where every person with OUD gets the best possible care and opportunity to reach their full potential. Our shared commitment to innovation on behalf of patients enables us to help people with OUD begin and sustain recovery. At Braeburn, there are opportunities to contribute to our purpose every day. We value authenticity and strive to amplify all voices. Our culture empowers everyone to be successful and unleashes our full potential.

Role Description Infinite Medical P.C. is seeking a highly motivated and passionate Medical Doctor Licensed in Cardiology to oversee and direct Nurse Practitioners who provide direct bedside care to nurses in geriatric facilities, ensuring the highest standards of patient care and contributing to the overall success of the organization. Responsibilities - Clinical Oversight of Nurse Practitioner - Monthly meetings/Check-ins with the assigned Nurse Practitioners - Staff Supervision of assigned Nurse Practitioners/Physician Assistants - Consult with the provider either onsite or via electronic communication (phone, email, etc) - Review provider notes and submit summaries for potential regulatory review Qualifications - Medical Degree - MD/DO - Board Certification - Current Licensure in Cardiology in the State of New York - Clinical Experience - Leadership Skills - Communication Skills - Commitment to Quality Improvement - Experience in a long-term care setting Requirements - Medical Degree - MD/DO - Board Certification - Current Licensure in Cardiology in the State of New York - Clinical Experience - Leadership Skills - Communication Skills - Commitment to Quality Improvement - Experience in a long-term care setting Benefits - This position is a contractor role, paid per collaboration, per month EEO/AAP Statement Infinite Medical P.C. is an equal-opportunity employer. We acknowledge and honor the fundamental value and dignity of all individuals. We pledge ourselves to crafting and maintaining an environment that respects diverse traditions, heritages, and experiences. Infinite Medical P.C. is an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based on race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.