1

Clinical Development Biotech Jobs in Arizona (NOW HIRING)

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... We create intelligent connections to accelerate the development and commercialization of innovative ...

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... We create intelligent connections to accelerate the development and commercialization of innovative ...

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... We create intelligent connections to accelerate the development and commercialization of innovative ...

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... We create intelligent connections to accelerate the development and commercialization of innovative ...

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... We create intelligent connections to accelerate the development and commercialization of innovative ...

Clinical Trial Psych Rater

Gilbert, AZ ยท Remote

$62K - $156K/yr

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... We create intelligent connections to accelerate the development and commercialization of innovative ...

Clinical Trial Psych Rater

Mesa, AZ ยท Remote

$62K - $156K/yr

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... We create intelligent connections to accelerate the development and commercialization of innovative ...

Showing results 21-40

Clinical Development Biotech information

What is clinical development in biotech?

Clinical development in biotech refers to the process of testing new drugs or therapies in human participants to determine their safety and effectiveness. This phase follows preclinical research and involves multiple stages of clinical trials, from Phase I (safety) to Phase III (efficacy and monitoring of side effects). Clinical development professionals coordinate the design, implementation, and analysis of these studies, ensuring compliance with regulatory standards. Their work is crucial in bringing innovative treatments from the laboratory to patients. Success in this field requires knowledge of medical science, regulatory guidelines, and project management.

What are the key skills and qualifications needed to thrive as a clinical development professional in biotech?

To thrive in Clinical Development within biotech, you need a strong background in life sciences, clinical trials management, and regulatory compliance, often supported by an advanced degree (e.g., PhD, PharmD, or MD). Proficiency with clinical trial management systems (CTMS), data analysis tools, and familiarity with ICH-GCP guidelines and FDA regulations are typically required. Strong project management, communication, and problem-solving skills help navigate complex studies and multidisciplinary teams. These competencies are essential to ensure safe, efficient, and compliant development of new therapies from concept to market.

What are the typical challenges faced by professionals working in clinical development within the biotech industry?

Professionals in clinical development for biotech companies often encounter challenges related to navigating complex regulatory requirements, managing tight timelines, and ensuring robust data quality across clinical trials. Additionally, frequent cross-functional collaboration is needed, as teams work closely with regulatory affairs, medical affairs, and data management to drive studies forward. Adapting to evolving scientific advancements and shifting project priorities are also common, so flexibility and strong communication skills are essential for success in this fast-paced environment.

What is the difference between Clinical Development Biotech vs Clinical Research Associate?

AspectClinical Development BiotechClinical Research Associate
Required CredentialsBachelor's or higher in life sciences, relevant certificationsBachelor's in life sciences, often with CRA certification
Work EnvironmentPharmaceutical/biotech companies, labs, clinical trial teamsMonitoring sites, clinical trial sites, sponsor offices
Employer & Industry UsageBiotech firms, pharmaceutical companies, CROsPharmaceutical companies, CROs, research organizations
Common Search & ComparisonYesYes

The Clinical Development Biotech role focuses on planning and managing clinical trials within biotech companies, often involving protocol development and regulatory submissions. In contrast, a Clinical Research Associate primarily monitors clinical trial sites to ensure compliance and data integrity. While both roles require similar educational backgrounds and certifications, their daily responsibilities and work environments differ, with the former being more involved in trial design and the latter in trial oversight.

What are popular job titles related to Clinical Development Biotech jobs in Arizona?

For Clinical Development Biotech jobs in Arizona, the most frequently searched job titles are:

What cities in Arizona are hiring for Clinical Development Biotech jobs?

Cities in Arizona with the most Clinical Development Biotech job openings:

Medical Science Liaison, IgG4 - Rare Disease - UT, AZ

Initial Therapeutics, Inc.

Phoenix, AZ โ€ข On-site

$120 - $180/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 19 days ago


Key responsibilities

  • Establish, develop, and maintain relationships with medical thought leaders, clinicians, and other external customers.

  • Communicate scientific and medical information about the company's products and therapeutic areas to the medical community and internal teams.

  • Support and participate in scientific conferences, identify external research opportunities, and facilitate clinical research collaborations.


Job description

Join Amgens Mission of Serving Patients

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Medical Science Liaison, IgG4 - Rare Disease Territory to includ e UT, AZ What you will do

Lets do this. Lets change the world. In this vital role you will serve as a scientific liaison to the medical/scientific community and will be responsible for establishing, developing and maintaining relationships with prominent experts and clinicians throughout the US.

  • Network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors, managed care decision makers, and pharmacy directors in alignment with applicable compliance, legal, and regulatory guidelines.

  • Understand, integrate and effectively communicate scientific/medical information and commercial value of products to the medical community and other key internal and external audiences.

  • Prioritize and work effectively in a self-directed manner in a constantly changing environment, including ability to obtain, integrate, and communicate customer feedback.

  • Pair customers unmet needs with available internal resources.

  • Collaborate effectively with all functional areas to identify opportunities and needs that can be addressed via communication of scientific, medical, and health economic information.

  • Identify potential new speakers and train on scientific content for sponsored external speaker programs.

  • Participate in national and regional conferences, meetings, and other scientific venues as appropriate to support the Medical/Clinical strategy and to obtain new competitive information, keep abreast of clinical trends, and support and maintain relationships with key investigators and scientific research.

  • Working in conjunction with the medical affairs and clinical development teams, evaluate potential external clinical research collaboration opportunities and facilitate the conduct of external clinical investigator-initiated trials (IITs) and company-sponsored trials.

  • Monitor the competitive environment for advances and trends in our therapeutic areas, including new treatment management and new therapies, as well as competitive products and features and provide feedback to the senior leadership team on specific initiatives of competitors.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a self starter with these qualifications.

Basic Qualifications:
  • Doctorate degree

OR

  • Masters degree & 3 years of Medical Affairs experience

OR

  • Bachelors degree & 5 years of Medical Affairs experience

Preferred Qualifications:
  • Pharm.D., Ph.D., M.D. or D.O. (other doctoral degrees considered)

  • 2 years of proven experience in scientific or medical affairs at a biotech or pharmaceutical company

  • Exceptional oral and written communication and interpersonal skills (including strong demonstration of ability to network) required.

  • Ability to travel up to 60% for territory management, attendance at regional and national conferences/workshops, and attendance at company meetings.

  • There may be a need to work up to 15-hour days due to travel

  • Must have ability to learn to use new business applications across hardware tools (e.g., PC, iPad).

  • Proficient in Microsoft Office.
  • Professional, proactive demeanor.
  • Strong interpersonal skills.
  • Excellent written and verbal communication skills.
What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts

  • A discretionary annual bonus program or for field sales representatives, a sales-based incentive plan

  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models, including remote and hybrid work arrangements, where possible

Sponsorship for this role is not guaranteed.

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Application deadline

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

#J-18808-Ljbffr