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Pharmd In Jobs in Tucson, AZ (NOW HIRING)

Roche

Global Clinical Program Lead

Tucson, AZ · On-site +1

$111K - $206K/yr

D., or PharmD) in a life sciences or clinical research discipline. * Project Management Professional (PMP) or equivalent project management certification. * Prior experience managing clinical ...

Roche Holding AG

Clinical Development Lead

Tucson, AZ · On-site

$125 - $150/hr

You hold a Doctoral or advanced degree (e.g., PhD, MD, PharmD) in life sciences, pharmacology, biomedical engineering, biostatistics/epidemiology, or a related clinical research field. * You bring 2+ ...

Roche

Clinical Development Lead

Tucson, AZ · On-site +1

$100K - $186K/yr

You hold a Doctoral or advanced degree (e.g., PhD, MD, PharmD) in life sciences, pharmacology, biomedical engineering, biostatistics/epidemiology, or a related clinical research field. * You bring 2+ ...

UnitedHealth Group

Staff Pharmacist Per Diem

Tucson, AZ · On-site

$44 - $79/hr

Pharmacy degree (BS or PharmD) from an ACPE accredited school of pharmacy * Current Arizona Pharmacist license in good standing * Experience using computer applications including word processing ...

UMR

Staff Pharmacist Per | , Arizona

Tucson, AZ · On-site

$44 - $79/hr

Pharmacy degree (BS or PharmD) from an ACPE accredited school of pharmacy * Current Arizona Pharmacist license in good standing * Experience using computer applications including word processing ...

Veracity

Pharmacist FT Rotating

Tucson, AZ · On-site

$56.25 - $67.50/hr

Participates in hospital safety/quality programs and assists in training new staff and students ... S. or PharmD degree. WORK EXPERIENCE Required : Must be able to work variable shifts including ...

divvyDOSE

Staff Pharmacist Per | , Arizona

Tucson, AZ · On-site

$44 - $79/hr

Pharmacy degree (BS or PharmD) from an ACPE accredited school of pharmacy * Current Arizona Pharmacist license in good standing * Experience using computer applications including word processing ...

UnitedHealth Group

Staff Pharmacist Per Diem

Tucson, AZ · On-site

$44 - $79/hr

Pharmacy degree (BS or PharmD) from an ACPE accredited school of pharmacy * Current Arizona Pharmacist license in good standing * Experience using computer applications including word processing ...

APC, Inc.

Pharmacist

Tucson, AZ · On-site

$60/hr

Bachelor of Science in Pharmacy (BS Pharm) or Doctor of Pharmacy (PharmD) degree from an accredited pharmacy school. * Current and unrestricted pharmacy license in the state of Arizona. * Strong ...

CVS Health

Grad Pharmacist

Green Valley, AZ · On-site

$21 - $42/hr

PharmD graduate of a U.S. accredited program prior to beginning Post-Graduate Training Program at CVS Health * 0-3 years prior relevant work experience * Must possess or be in process of obtaining a ...

CVS Health

Grad Pharmacist

Tucson, AZ · On-site

$21 - $42/hr

PharmD graduate of a U.S. accredited program prior to beginning Post-Graduate Training Program at CVS Health * 0-3 years prior relevant work experience * Must possess or be in process of obtaining a ...

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All JobsPharmd In JobsPharmd In Jobs in Tucson, AZ

Pharmd In information

What is a PharmD in India?

A PharmD in India is a Doctor of Pharmacy degree, which is a professional doctoral program in pharmacy. It typically spans six years, including five years of academic study and one year of internship or residency. The program is designed to train students in clinical pharmacy, patient care, and medication therapy management, preparing them to work as clinical pharmacists in hospitals, healthcare settings, or pursue further research or academic opportunities. PharmD graduates are eligible for roles that involve direct patient care and can also pursue registration as pharmacists in India.

What do PharmD in inpatient hospital settings do?

As a PharmD working in an inpatient hospital, you will routinely collaborate with physicians, nurses, and other healthcare professionals to optimize medication therapy for patients. This often includes participating in patient rounds, reviewing medication orders for accuracy and safety, providing drug information, and making evidence-based recommendations to the care team. You may also assist in medication reconciliation and discharge planning to ensure continuity of care. Building strong interdisciplinary relationships is key to improving patient outcomes and ensuring safe medication practices.

What are the key skills and qualifications needed to thrive as a PharmD in industry?

To thrive as a PharmD in industry, you need a Doctor of Pharmacy degree, a strong grasp of pharmacology, regulatory knowledge, and often licensure as a pharmacist. Familiarity with drug development software, regulatory databases, and certifications like RAC (Regulatory Affairs Certification) are commonly required. Excellent communication, analytical thinking, and collaboration skills help you effectively manage projects and interact with cross-functional teams. These competencies ensure regulatory compliance, drive innovation, and contribute to the safe and efficient development of pharmaceutical products.

What is the difference between Pharmd In vs Pharmacist?

AspectPharmd InPharmacist
CredentialsDoctor of Pharmacy (PharmD) degree, licensureDoctor of Pharmacy (PharmD) degree, licensure
Work EnvironmentInternship, training, or entry-level roles in pharmacies or healthcare settingsLicensed practice in retail, hospital, or clinical pharmacy settings
Employer & IndustryPharmacy schools, healthcare facilities, internshipsCommunity pharmacies, hospitals, clinics

Pharmd In typically refers to students or trainees in pharmacy programs or those in early training stages, whereas Pharmacist denotes a fully licensed professional practicing in various healthcare settings. Both roles require the PharmD degree and licensure, but Pharmd In is often associated with educational or internship phases, while Pharmacist indicates full professional practice.

Is a PharmD in demand?

A PharmD is in high demand due to the ongoing need for pharmacists in healthcare settings, including hospitals, retail pharmacies, and clinics. The profession requires strong knowledge of medications, patient care, and often licensure, with job growth expected to remain steady as the healthcare industry expands.

Is a Pharmd worth it?

A PharmD degree prepares individuals for careers as pharmacists, a profession that typically offers stable employment, competitive salaries, and opportunities in healthcare settings. The degree requires completing a rigorous curriculum, passing licensing exams, and often involves clinical experience, making it a valuable credential for those interested in pharmacy practice.
Pharmd In jobs near you

Clinical Development Lead

Tucson, AZ • On-site

F. Hoffmann-La Roche Ltd
See more jobs at F. Hoffmann-La Roche Ltdexternal

$100K - $186K/yr

Full-time

Posted 12 days ago

Key responsibilities

  • Lead the development and management of clinical documentation, including protocols, study reports, and regulatory submissions.

  • Collaborate with cross-functional teams to support study design, data synthesis, and regulatory compliance.

  • Mentor junior team members and support process improvements in medical and scientific writing.

Job description

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The Position
A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche.
The Opportunity
As a Clinical Development Lead (Medical & Scientific Writing), you will serve as a strategic partner within our Clinical Evidence for In-Vitro Diagnostics (CEI) team to drive clinical evidence generation and study design for cutting-edge In-Vitro Diagnostics (IVD). In this role, you will lead end-to-end documentation strategy and lifecycle management to support regulatory submissions and advance patient care across key disease areas including Infectious Diseases, Oncology, and Cardiovascular/Metabolic Diseases.
  • Design scientifically sound clinical protocols in close partnership with Subject Matter Experts (SMEs) to support novel IVD product development and regulatory filings.
  • Author, review, and finalize critical clinical study documents, including protocols, Clinical Study Reports (CSRs), Investigator Brochures, and IVDR Performance Evaluation documentation.
  • Conduct comprehensive scientific literature reviews and synthesize complex multi-modal laboratory and clinical data into clear, regulatory-ready reports.
  • Drive end-to-end document lifecycle management, ensuring compliance with internal procedures, quality control standards, and international regulatory requirements.
  • Partner cross-functionally with Medical Affairs and Scientific Communications to support manuscript, poster, and advisory board content generation.
  • Mentor junior members of the Medical Writing team, championing process improvements, document automation, and collaborative best practices.

Who you are (Required)
  • You hold a Doctoral or advanced degree (e.g., PhD, MD, PharmD) in life sciences, pharmacology, biomedical engineering, biostatistics/epidemiology, or a related clinical research field.
  • You bring 2+ years of proven scientific research and medical/scientific writing experience in an industry or academic setting, with direct experience authoring clinical protocols and reports.
  • You possess a strong track record of publications in peer-reviewed scientific journals.
  • You demonstrate strong organizational, project management, and cross-functional communication skills, with a proven ability to lead multiple complex projects simultaneously.
  • You are highly proficient in common word processing, document lifecycle management, and collaborative software tools.

Preferred
  • 3+ years of specialized experience in regulatory/medical writing specifically for In-Vitro Diagnostics (IVD), companion diagnostics, or medical devices.
  • Demonstrated experience with IVD-Regulation (IVDR) performance evaluation documentation and regulatory agency submission responses.
  • Familiarity with clinical laboratory techniques including PCR, next-generation sequencing (NGS), immunohistochemistry (IHC), or immunological assays.
  • Basic understanding of biostatistical methods and clinical trial data evaluation.
  • Direct experience in project management or mentoring junior team members.

Location
  • This position may be based out of Tucson (Arizona, USA) or Indianapolis (Indiana, USA) with remote work locations possible.
  • No relocation benefits are available for this posting.

Travel Requirements
  • Occasional domestic travel to select conferences or internal meetings.

The expected salary range for this position based on the primary location of AZ is $100,500 - $186,700. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits
Who we are
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

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