Regulatory Trailblazers: Early Talent Program
F. Hoffmann-La Roche AG
Genentech, a Roche company, invites applications for the Regulatory Early Talent Program. This two-year contract offers hands-on regulatory work, mentorship, and exposure to global teams, focusing on foundational regulatory deliverables and health authority interactions. Candidates should hold a life sciences degree and be within two years of completion, with minimal pharma experience. Start is May 2027, based in South San Francisco, full-time on-site, with relocation not offered and paid #J-18808-Ljbffr F. Hoffmann-La Roche AG
- Genentech seeks candidates for the Regulatory Early Talent Program - OnePDR, a two-year contract designed to build foundational regulatory experience through hands-on assignments and tailored learning solutions. Participants collaborate with global drug development teams...RegulatoryContract work
$56.8k - $105.6k
The Position Regulatory Early Talent Program - OnePDR The Position This is a temporary, 2-year contract position. Embark on a transformative two-year journey with the One Product Development Regulatory (PDR) Early Talent (ET) Program, meticulously crafted to impart comprehensive...RegulatoryFull timeTemporary workWork at officeLocal areaWorldwideRelocation package$148k - $185k
...Senior Project Manager, Biologics R&D - Early Pipeline Programs About Xaira Therapeutics Xaira is an innovative biotech startup focused... ...; familiarity with downstream nonclinical, CMC, and regulatory components is a plus. Strong analytical, planning, and...RegulatoryFor contractorsWork at officeRemote workFlexible hoursShift work- ...Job Summary: The Early Phase program has a multi-disciplinary team that works closely with... ...guidelines of research protocols and regulatory policies. The CRC will assist in the care... ...community made of people with many skills and talents. We seek candidates whose work...RegulatoryFull timeWork experience placementWork at officeLocal areaWorldwide
$165.1k - $306.5k
...makes us Roche.This role is in Early Development Biometrics (EDB),... ..., and implement high-quality programming and analytical solutions to... ...exploratory analyses, early regulatory engagements, and complex data... ...drives continuous improvement, talent development, and a culture of...RegulatoryFull timeLocal areaFlexible hours$212.7k - $374.4k
...and we're looking for Trailblazers who are passionate about... ...Financial Services Program Executive (PE) is a senior... ...of our most senior talent across our most complex... ...of surfacing issues early enough to course-correct... ...on industry trends, regulatory considerations, and the...RegulatoryFull time- ...quality educational opportunities from early childhood through higher education, health... ...:This position reports to the Program Manager, Early Care and Education Program... ...repairs, space planning, health and safety, regulatory compliance, and business planning.Assist...RegulatoryCasual workWork at officeLocal areaRemote workAfternoon shift2 days per week
- ...treatments. We are currently seeking a Regulatory Affairs Director to join our growing regulatory... ...the development of multiple oncology early development assets, contributing to the... ...of regulatory documentation Support non-program specific projects assigned such as...Regulatory
$176k - $215k
Senior Clinical Trial Manager, Early Development Join to apply for... ...plans with scientific and regulatory objectives. Lead study feasibility... ...led by two wholly owned lead programs, MZE829 and MZE782, each of... ...and the development of talent. Our supportive work environment...RegulatoryFull timeContract workInterim role- ...This senior leadership position manages clinical development programs from early through late-stage trials, serving as the central... ...trials progress on schedule and within budget while maintaining regulatory compliance. Responsibilities Lead strategic and operational...Regulatory
- ...AstraZeneca seeks a Global Clinical Program Lead to oversee clinical development and execution... ...strategic planning, team leadership, regulatory submissions, and cross-functional... ...7 years drug development experience in early and late phase programs Strong hematology...Regulatory
- ...Vice President, Early Clinical Development, Oncology About the Company Innovative... ...portfolio, with a focus on advancing programs from discovery into the clinic. The successful... ...essential, as is a strong background in regulatory interactions. The role demands excellent...Regulatory
- Role: Global Clinical Program Lead, Hematology Hybrid Working: Minimum... ..., and we nurture and build talent. Within Hematology R&D, we... ...rapid acceleration of promising early-stage assets and life-cycle... ...leading to drug approval by regulatory agencies (Phase 1, 2 and 3 trials...RegulatoryHourly payTemporary workWork at office3 days per week
$424.15k
...targets and leads, respectivelyWorking with Early Clinical Development to translate novel... ...research activities comply with relevant regulatory requirements and ethical standardsThis... ...FOR THIS ROLETeam Leadership, Attracting Talent and Developing People: Fosters high-performing...RegulatoryFull timeLocal areaShift work- ...AbbVie seeks a Manager of Statistical Programming to lead a team of statistical programmers... ...programming activities, ADaM dataset creation, regulatory documentation, and team management in a... ...for compounds or therapeutic areas in early development Manage team of...Regulatory
- ...Senior Medical Director role overseeing early-phase oncology clinical development programs at a pharmaceutical company. Leads cross-functional teams in designing and executing clinical trials, managing regulatory submissions, and interpreting safety and efficacy data...Regulatory
$190k - $225k
...1 monotherapy data from this program across multiple solid tumor types... ...’s beyond. The Principal Talent Acquisition Partner, R&D and... ...Development and Operations, Regulatory Affairs, Research, Quality,... ...opportunities, and decision criteria early in the recruiting process...RegulatoryImmediate startRelocationFlexible hours- Scorpion Therapeutics is seeking a Senior Director of Program Management to lead cross-functional drug development programs from strategy... ...role requires coordinating timelines and aligning clinical, regulatory, CMC, nonclinical, and commercial plans while managing risks...Regulatory
$270k - $325k
POSITION SUMMARY: The Senior Director, Program Management is a senior cross-functional leader... ....This role works across clinical, regulatory, CMC, nonclinical, commercial and other... ...broader program.Identify major program risks early and work with accountable functions to...RegulatoryRemote workFlexible hours- dawarconsulting is seeking a Senior Program Director of Commercial Regulatory Affairs to lead PRC meetings, review promotional materials, and provide FDA compliance guidance. You will collaborate with Marketing, Medical, Legal, and Compliance teams to ensure accurate regulatory...RegulatoryRemote jobLong term contract
$120.2k - $223.2k
The PositionCommercial Regulatory Affairs (CORA) is part of the Global Product and Access Legal (GPAL) organization that interprets the... ...Head of GPAL in the Global Legal Pharma Department.Associate Program Directors of Commercial Medical Legal Regulatory Review Committees...RegulatoryFull timeWork experience placementLocal areaWorldwideRelocation package- ...most important and ambitious deployment programs, with multiple launches requiring close... ...supply chain, construction, logistics, regulatory, software, operations, finance, and country... ...and global teams, you’ll identify risks early, drive accountability, resolve cross-...RegulatoryLocal area
$175k
...clients. The 10-week Summer Associate Program is designed for MBA students between... ...must also meet and comply with ongoing regulatory obligations, which include periodic screening... ...31 Jan 2027* Job posting may come down early due to volume of applicants. We Value...RegulatorySummer workInternshipWork at office$154.2k - $192.8k
...Quality Control, Learning & Development, and Program Management, and supports Fraud &... ...Lead Bank Charter ReadinessTranslate the regulatory expectations of a chartered bank (Reg E,... ...from scratch where none exists.Raise risks early, make trade-offs explicit, and drive...RegulatoryImmediate start$283k - $325k
...Position Summary:Structure is seeking a talented, strategic, and highly motivated... ...readiness across the company’s early and late-phase clinical development programs. With a primary focus on Phase 3... ..., inspection planning, and regulatory inspections, this individual will...RegulatoryContract work$230k - $270k
...motivated Senior Director, CMC Regulatory Affairs in the Global... ...innovative Allogeneic CAR T programs. Provide CMC expertise for... ...regulatory submissions from early development to pre and post approval... ...offer a chance to work with talented people in a collaborative environment...RegulatoryFull timeContract workInternshipLocal areaRemote work2 days per week$148k - $185k
...manager of record for our lead T-cell engager program, as it advances from late-stage research... ...across research, nonclinical, CMC, and regulatory workstreams. Build and maintain project... ...and failure modes for biologics early development (e.g., developability, cell...RegulatoryWork at officeRemote workFlexible hoursShift work- AstraZeneca seeks a Global Clinical Program Lead in Hematology to drive the clinical development plan and execution across multiple... ...leaders and external experts to deliver integrated plans that meet regulatory and portfolio objectives. The successful candidate will have M...Regulatory
$390k
...the benefit of patients with cancer. Our programs take novel approaches to shutting down... ...interactions, and filings. Contribute to global regulatory filings and health authority... ...authorities required. ~ Exposure to early development and the transition from FIH...RegulatoryTemporary workCasual workLocal areaWorldwideFlexible hours- ...leading clinical development for pancreatic and colorectal cancer programs at a precision oncology company. Reports to Chief Medical... ...medical oversight of drug development strategy, trial design, regulatory filings, and cross-portfolio clinical decision-making. Responsibilities...Regulatory
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