Saad A. Email & Phone Number

Devon, Pennsylvania, Us

As a Senior Consultant in Strategic Engagement, I specialize in developing and executing strategies to enhance stakeholder engagement and optimize market access for pharmaceutical and biotech products. I collaborate with cross-functional teams to deliver tailored insights, driving value-based care initiatives and aligning strategies with evolving US healthcare trends. My focus includes US payer and provider engagement, market access optimization, and supporting clients in navigating the complexities of the US healthcare landscape to improve product success and patient access

Raritan, Nj, Us

As Director of New Business Development, Global Pricing, & Market Access, I led strategic initiatives to expand market presence and optimize patient access to innovative therapies. I managed cross-functional teams in developing tailored market access and pricing strategies for global pharmaceutical and biotechnology clients, focusing on areas such as orphan diseases, oncology, and biosimilars. With a strong business development acumen, I oversaw new client acquisitions, built key stakeholder relationships, and delivered data-driven solutions that supported successful product launches and long-term market growth for the organization

Raritan, Nj, Us

As a Senior Analyst/Manager at Market Access Solutions LLC, I led high-performing teams in optimizing patient access to innovative healthcare solutions. I designed and implemented comprehensive market access research strategies, collaborating closely with payers and providers to extract critical insights. By delivering data-driven, value-enhancing recommendations, I empowered stakeholders to make informed, strategic decisions that drove product success and improved patient outcomes.

Bagsværd, Dk

In my role at Novo Nordisk Inc. (NNI), I focused on verifying adverse events (AEs) and associated technical complaints (TCs) related to glucagon-like peptide-1 (GLP-1) and biopharmaceutical portfolios. I ensured the completeness and seriousness of case narratives, assessed product coding, medical history, indications, and adverse events, and conducted label assessments. Collaborating with fellow case handlers, I provided ongoing feedback to support their development. Additionally, I processed and analyzed AEs and associated TCs from NNI products into the company's (CCGlow) and global safety databases (Argus). I addressed product inquiries using approved labeling and worked closely with cross-functional teams, including the Patient Care Call Center, Medical Information, Legal, and other stakeholders, to obtain and process safety data effectively.

Browns Mills, New Jersey, Us

In my time as a Clinical Pharmacist at Deborah Heart & Lung Center, I played a vital role in the development of content for left ventricular assist device (LVAD) and pulmonary hypertension programs. I formulated protocols for anticoagulation, infection control, right ventricular failure, and comfort care, ensuring comprehensive patient care. Additionally, I established a medication use and administration guide for off-label use of inhaled epoprostenol. Collaborating with cross-functional colleagues, I contributed to formulary decision making, evaluating treatments for pulmonary hypertension. I designed order sets, documentation methods, and IV pump settings, streamlining processes and enhancing patient care. Delivering clinical presentations and competency assessments, I effectively educated pharmacy and intensive care unit staff. My expertise extended to delivering relevant drug information to various healthcare professionals and making patient-specific pharmacotherapy recommendations based on factors such as age, weight, renal function, and comorbidities. Moreover, I oversaw therapeutic drug monitoring for patients requiring medications like vancomycin, phenytoin, gentamicin, and others.

Woonsocket, Rhode Island, Us

• Enhanced patient outcomes in collaboration with other healthcare professionals.• Interfaced with patients on proper medication usage and over the counter medications.• Directed and monitored pharmacy technicians, ensured proper execution of daily pharmacy tasks.

Princeton, Nj, Us

• Assisted on various abstracts, slide decks, posters, regulatory documents and manuscripts for clients. Areas of work included oncology, women’s health, connective tissue disorders, and biosimilars.• Supported publication planning, medical strategy, and advisory board meetings. • Drafted executive summaries, highlighting company services available for the potential client. • Reviewed data for accuracy for medical communications content with approaching deadlines. • Formalized and designed website structure and developed content for clinical trial recruitment program.

Summit, New Jersey, Us

• Identified, disseminated, and evaluated key literature for Abraxane® (protein-bound paclitaxel), including safety/efficacy, dose modification, and health economics outcomes research data. • Maintained and updated medical response documents for unsolicited medical information requests. • Devised and developed on-going study tracker for Abraxane® usage in pancreatic cancer. • Evaluated and compared recommendations for Abraxane® in ASCO and NCCN guidelines, as well as UpToDate. • Contributed to various promotional review meetings for the approval of commercial information.

• Launched medication waste protocols and educated nurses regarding Drug Buster® and ContraPatch™.• Spearheaded anti-microbial stewardship program in collaboration with infectious disease physicians. • Reviewed and revised therapeutic interchange policy with formulary approved fluoroquinolones and carbapenems. • Dosed medications such as warfarin, vancomycin, piperacillin/tazobactam, and gentamicin. • Monitored and tracked nephrotoxic antibiotics to determine the correlation between use and discontinuation.

Philadelphia, Pa, Us

• Participated in rounds with residents, interns, and attending hospitalists in the step-down unit. • Addressed inquiries and delivered in-depth responses to complex drug information questions.• Recommended various patient-specific drug therapy plans based on disease state, cost, and quality of life.• Furnished unique patient cases and medication therapy presentation to nurses, pharmacists, and physicians.

• Administered in-depth patient interviews for primary care, anticoagulation, and psychiatry departments. • Developed customized treatment plans including lifestyle modifications, insulin regimens, and medication adjustments. • Headed intensive outpatient rehabilitation programs regarding smoking cessation and substance abuse.• Observed patients’ INRs using Coaguchek® and adjusted based on readings when necessary.

Summit, New Jersey, Us

• Managed safety data to support team efforts for Otezla® (apremilast) and Revlimid® (lenalidomide).• Examined safety sections of trial protocols against protocol template and identified differences.• Generated line listings, frequency reports, and CIOMS reports from ARISg database. • Considered and assessed new cases for internal discrepancies and liaised with case management on corrections.• Customized medication specific slide decks for investigator training meetings. • Composed, developed, and modified key documents required for ongoing clinical trials, including Serious Adverse Event (SAE) reporting plan, reporting form, and completion guidelines. • Scrutinized adverse event reports from drug safety database to detect trends in overall data.

Doctor Of Pharmacy - Pharmd, Pharmacy

Bachelor'S Degree, Pharmaceutical And Healthcare Sciences