Sr Mgr Clinical Development

Date: May 22, 2026

Location:

Buenos Aires, Argentina, 00000

Company: Teva Pharmaceuticals

Job Id: 67936

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

Senior Manager, Clinical Development (Clinical Development Scientist (CS)) provides input into a clinical study protocol and supports a clinical study team. The CS provides scientific expertise necessary to design and deliver clinical studies and programs and supports assigned clinical development physician, the clinical leader, and disease area (DA) head with deliverables necessary for effective and efficient clinical study design and execution.

How You’ll Spend Your Day

- Support the development of the protocol concept sheet, protocol and protocol amendments, Clinical Study Report and other clinical documents.
- Contribute to the development, writing and review of the Clinical Development Plan.
- Provide appropriate scientific and clinical input and support for all activities related to clinical studies: e.g., clinical development team activities, investigators training, site feasibility, patients eligibility, Medical Management Plan, clinical review of data, IDMC and IAC activities and more.
- Activities related to data generation and validation, including(case report form) design, clinical data review/query resolution. Ensure continuous medical review of aggregated data during clinical trial conduct to identify trends and ensure quality data for database locks and interim data reviews.
- Author or contribute to the development or review of medical related study documents (e.g., pre-defined protocol deviation list, the Informed Consent Form, narrative plan, study specific committee charter).
- Support CRAs/CROs and internal Teva personnel on study protocol and related questions. Serves as point of contact for managing/answering questions relating to trial procedures.
- Contribute to the processing of responses to inquiries raised by EC/IRBs, sites and health authorities.

Your Skills and Experience

Education: Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or another scientific field preferred). Strong scientific background.

Experience: Minimum of 2 years of experience in clinical research within pharmaceutical industry or CRO, or equivalent specifically in clinical study design, data analysis, data review and interpretation.
• Independently perform scientific literature searches, read and understand scientific and medical/clinical concepts and analyze relevant quality peer reviewed data.

Skills: Understand phase I-III drug development including knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and clinical development concepts/processes.
• Demonstrates knowledge and application of statistical analysis methodology and can identify data trends and interpret data effectively through the continuum of a study.
• Strong knowledge of Therapeutic/Disease Area (TA/DA), with the capability to interpret, discuss and present trial or program level data.
• Maintain knowledge of the disease area, disease state and potential drug effects

Language: Excellent scientific communication skills, both verbal and in writing English

Also Good to Have

How We’ll Take Care of You

At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community.  When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way. 

Already Working @Teva?

Make sure to apply through our internal career site on Twist—your one-stop shop for career development

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.