Director - ADME Job at Enveda (Hyderabad)

Scientific Associate Director - Pharmacokinetics and Drug Metabolism

In this vital and exciting role, you will oversee Pharmacokinetics and Drug Meta...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

PhD in Pharmacokinetics, Pharmaceutical Sciences, Engineering, or related fields with equivalent professional degrees and 12+ years of experience in the Biotechnology/Pharmaceutical Industry
Solid technical experience with the application of SM in vitro/in vivo ADME and pharmacokinetics fundamentals to drug discovery projects
Ability to drive the progression of SM discovery and development within project teams
Expertise with in vitro ADME, in vivo ADME, PK/PD etc
Experience in supporting preclinical components of regulatory documentations
Excellent interpersonal, technical, and communication skills
Past experience as a laboratory scientist in a pharma or biotech environment
Excellent written and oral communication skills, attention to detail and accuracy, and interpersonal skills
Record of scientific contributions through peer-reviewed articles and external presentations

Job Responsibility

Lead/mentor a team of scientists involved in ADME characterization of small molecules
Directly responsible for leading a team of scientists involved in undertaking mechanistic in vitro ADME assays
Develop/implement novel tools to efficiently support mechanistic ADME work
Oversee activities/establish workflows for small molecule bioanalytical and ADME screening teams
Serving as a subject matter expert of small molecule ADME to support the programs and recommend strategies to PKDM project team representatives to reduce/mitigate risks due to metabolism
Collaborate with scientists across our PKDM scientific community
Leveraging specialized ADME/PK skills such as in vitro ADME, in vivo ADME, biotransformation, PK/PD, to impact project progression and decision-making
Contributing to the analysis of pre-clinical ADME and PK data for IND and NDA filings and documenting these analyses in appropriate reports
Building close relationships with partner functions

New

Director, Clinical Pharmacology

The role is positioned in the Clinical Pharmacology group, Clinical and Quantita...

Location

United States , Cambridge

Salary:

167000.00 - 300700.00 USD / Year

Moderna

Expiration Date

Until further notice

Requirements

PhD and/or PharmD in Clinical Pharmacology, Pharmacometrics, Pharmaceutics, Statistics, Engineering, or a related field with a minimum of 8-10 years of industry experience in clinical pharmacology
In depth knowledge of clinical pharmacology, PK/PD principles, modeling and simulation, ADME and quantitative translational sciences
Hands-on quantitative skills, modeling expertise and familiarity with clinical operations and translational sciences
Sound knowledge of drug regulatory authority biopharmaceutics and clinical pharmacology requirements to support the clinical development and marketing of new drug products
Drug development experience in oncology and rare diseases preferred
expertise in immune therapeutics and/or infectious diseases is a plus
Platform expertise in mRNA therapeutics, and/or experience with biologics and new modalities preferred
Demonstrated ability to work independently, lead functional initiatives, adapt quickly and collaborate effectively in a highly dynamic environment and influence cross-functional teams
Proficient in using pharmacokinetic, modeling and data visualization software (e.g. Phoenix WinNonlin, R, Monolix, NONMEM, etc)
Outstanding verbal and written communication skills, with the ability to distill complex data for diverse audiences

Job Responsibility

Develop a fit-for-purpose Clinical Pharmacology development plan, including dose selection and optimization, evaluation plan for special populations, PK/PD and immunogenicity assessment, and pediatric development
Collaborate with program teams to develop dose selection strategy and support decision makings for first-in-human studies and IND submissions
Represent CQP in a highly matrixed team setting to drive study execution and operational excellence toward product development goals
Lead the development of CQP related sections in regulatory documents (e.g., clinical protocols, INDs, regulatory meeting briefing books, summary documents for BLAs, responses to regulatory authorities) and represent clinical pharmacology in regulatory interactions
Lead/oversee the Clin Pharm data analysis, interpretation, and reporting to inform clinical implications and development decisions
Advocate and represent clinical pharmacology and MIDD strategies with internal and external stakeholders
Mentor junior team members to contribute to the development of a high-performing Clinical Pharmacology team
Leverage literature data and collaborate with external consultants, CRO partners and academic sites to problem solve and develop solutions to clinical pharmacology issues and grow organizational knowledge on mRNA platform

What we offer

Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
Family planning benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investment opportunities to help you plan for the future
Location-specific perks and extras
Annual discretionary bonus, other incentive compensation, or equity award

Fulltime

New

Senior Director - Head of DMPK/ADME

Zealand Pharma is expanding its Drug Metabolism and Pharmacokinetics (DMPK) capa...

Location

Denmark , Søborg

Salary:

Not provided

Life Science Talent

Expiration Date

May 24, 2026

Requirements

PhD in pharmaceutical sciences or similar with extensive relevant industry experience.
Extensive experience addressing DMPK challenges for multiple modalities
Proven people-leadership experience, including building, mentoring and developing high-performing scientific teams across sites and/or in matrix environments
Experience contributing to regulatory-facing DMPK content (e.g., IND/CTA support, responses to agency questions)
Demonstrated ability to set DMPK strategy aligned with project and portfolio priorities, balancing scientific rigor with speed and resource constraints
Experience ensuring quality, compliance and scientific rigor in nonclinical assay validation oversight, sample analysis oversight, and vendor/CRO interactions

Job Responsibility

Provide strategic leadership and oversight for DMPK / ADME strategy and execution across the portfolio
Build, mentor, and scale DMPK capabilities, talent, and ways of working at the Boston site, ensuring strong alignment and integration with Copenhagen standards and interfaces
Oversee bioanalytical method development, including robust nonclinical assay validation and oversight of sample analysis (internal and external)
Lead in vitro ADME activities, including stability and drug–drug interaction (DDI) assessments, ensuring fit‑for‑purpose study design, interpretation, and documentation
Oversee in vivo pharmacokinetics and metabolite identification, integrating findings into a coherent ADME understanding and risk‑based decision framework
Deliver high‑quality nonclinical PK summaries and integrated DMPK data packages to support project decision‑making, governance processes, and external‑facing documentation as required
Drive continuous improvement through the implementation of automation, digital, and AI enabled approaches within DMPK workflows
Provide scientific leadership in cross functional project teams, partnering closely with Discovery, Translational, Clinical Pharmacology, Toxicology, and Regulatory colleagues
Ensure effective oversight of external partners and CROs, including scientific quality, timelines, and budget accountability
Contribute to regulatory strategy and interactions by ensuring DMPK content is scientifically sound and inspection ready

Fulltime

Director of Agency Development

Orchid Insurance, an Arrowhead Intermediaries company, is seeking a Director of ...

Location

United States , Tampa

Salary:

Not provided

Brown & Brown UK

Expiration Date

Until further notice

Requirements

Minimum of 7 plus years P&C industry experience
Minimum of 5 plus years of experience in account management, agency development, outside sales experience, or similar role
Demonstrates strong leadership qualities such as the ability to inspire and motivate others, effective decision-making, and a proactive approach to problem-solving
Passion to remove obstacles and get the job done
Possess a professional demeanor in a fast-paced production environment
Be willing to always represent the company with the utmost professionalism
Must be team-oriented and able to meet team deadlines
Must be results-oriented and thrive in high volume environments
Proficiency in MS Office Suite and CRM software such as Salesforce
Positive attitude and friendly demeanor

Job Responsibility

Under the direction of Distribution Management, responsible for the performance of the agency development team and is expected to achieve results through consistent recruitment, training, and supervising activities
Ensure proper staffing goals are met, and manage activities associated with the selection and performance of new agency development managers
Support the training and education of products across the team, including Personal Lines E&S and Digital partnerships
Support ADMs in managing territory operation and implementing action plans to meet or exceed goals and objectives
Generate new premium growth through coaching interactions with ADMs (calls, emails, f2f visits, etc.)
Cultivate relationships with new and existing assigned agents to direct qualified risk selection
Implement proactive efforts including activities that keep agents informed on systems, products, and underwriting guidelines as well as prospecting new agencies and general account management
Provide general account management for agencies and maintain accurate records of all sales activities via Salesforce – enforce usage of Salesforce by ADMs
Proactively monitor key performance indicators outlier, shares best practices and be solutions oriented
Monitor and report newly appointed agency metrics such as quote volume and written premium

What we offer

Health Benefits: Medical/Rx, Dental, Vision, Life Insurance, Disability Insurance
Financial Benefits: ESPP
401k
Student Loan Assistance
Tuition Reimbursement
Mental Health & Wellness: Free Mental Health & Enhanced Advocacy Services
Beyond Benefits: Paid Time Off, Holidays, Preferred Partner Discounts and more

Fulltime

Director, Medicinal Chemistry

Enveda is looking for a Director, Medicinal Chemistry to join our team in Hydera...

Location

India , Hyderabad

Salary:

Not provided

Enveda

Expiration Date

Until further notice

Requirements

Doctor of Philosophy in Synthetic Organic Chemistry
15-20 years of post-PhD experience in Medicinal Chemistry
Proven track record of delivery of leads and clinical candidates to the pharmaceutical industry
Management and mentoring of synthetic chemists
Good understanding of intellectual property of medicinally valuable compounds with respect to composition of matter, method of use and chemical processes
Strong understanding of safety practices in organic synthesis laboratories

Job Responsibility

Lead medicinal chemistry activities for two or more projects in parallel
Involved in identifying pre-leads, design and optimization of leads for potency, selectivity and druggability and also strong IP generation
Recruit PhD and M. Sc. synthetic chemists and mentor them as medicinal chemists and manage their performance and improve their productivity
Collaborate with peers in Medicinal Chemistry and work as a team to increase delivery of compounds to the Clinical Pipeline
Collaborate with Senior Leaders in other functional departments such as ADME, Analytical Sciences and Pharmacology and deliver high value molecules
Report to the VP, Discovery Chemistry
Collaborate on Medicinal Chemistry of Lead Generation and Lead Optimization of Pipeline Projects
Understand Structure Activity Relationships and Structure Property Relationships of various projects
Collaborate with Medicinal Chemistry, Pharmacology, Analytical, ADME, Tox, IP, Site and Global Leadership
Develop appropriate flow schemes with relevant in vitro, in vivo, ADME/PK and tox studies

What we offer

Culture
Medical
Block Leaves
Work-Life Harmony

Fulltime

Citrix Expert Consultant

Inetum is looking for a skilled Citrix Expert Consultant to join our team and su...

Location

Portugal , Lisbon

Salary:

Not provided

Inetum

Expiration Date

Until further notice

Requirements

Minimum of 5 years' experience in a similar Citrix-focused role
Solid expertise in Citrix CVAD, NetScaler (Citrix ADC), Citrix ADM, and Citrix Workspace Environment Management
Hands-on experience with ControlUp for dashboard management, analysis and automation
Strong knowledge of networking concepts (DNS, DHCP, load balancing, SSL VPNs)
Proficient in PowerShell scripting
Ability to diagnose and resolve complex technical issues
Excellent communication and collaboration skills
Fluent in English (B2–C1 level)

Job Responsibility

Design, deploy and manage Citrix Virtual Apps and Desktops (CVAD) environments across on-prem, hybrid and cloud infrastructures
Configure and maintain NetScaler (Citrix ADC) for load balancing, secure remote access, and application delivery
Implement advanced features such as TLS VPNs, MFA authentication, and performance tuning
Use ControlUp for real-time monitoring, troubleshooting, reporting, and process automation
Conduct performance reviews, collect feedback, and implement user experience improvements
Monitor Citrix platforms using tools such as Citrix Director and ControlUp Insight
Document processes and configurations to ensure consistent service quality
Collaborate closely with Infrastructure teams (Network, Wintel, Security) and business stakeholders
Provide technical support, training and guidance to users and internal IT teams
Ensure compliance with internal and external security standards and best practices

Fulltime

New

Pharmacy Technician

We’re building a world of health around every individual — shaping a more connec...

Location

United States , Drexel Hill

Salary:

Not provided

CVS Health

Expiration Date

June 22, 2026

Requirements

Must comply with any state board of pharmacy requirements or laws governing the practice of pharmacy, which includes but is not limited to, age, education, and licensure/certification
If the state board of pharmacy does not address or mandate a minimum age requirement, must be at least 16 years of age
If the state board of pharmacy does not address or mandate a minimum educational requirement, must have a high school diploma or equivalent, or be actively enrolled in high school or high school equivalency program
State-level licensure and national certification requirements vary by state, click here to learn more
Regular and predictable attendance, including nights and weekends
Ability to complete required training within designated timeframe
Attention and Focus
Customer Service and Team Orientation
Communication Skills
Mathematical Reasoning

Job Responsibility

Living our purpose by following all company SOPs at each workstation to help our Pharmacists manage and improve patient health
Following pharmacy workflow procedures at each pharmacy workstation (i.e., production, pick-up, drive-thru, and drop-off) for safe and accurate prescription fulfillment
Contributing to positive patient experiences by showing empathy and genuine care
Completing basic inventory activities, as permitted by law, and as directed by the pharmacy leadership team
Contributing to a high-performing team, embracing a growth mindset, and being receptive to feedback
Remaining flexible for both scheduling and business needs, while contributing to a safe, inclusive, and engaging team dynamic
Understanding and complying with all relevant federal, state, and local laws, regulations, professional standards, and ethical principles
Delivering additional patient health care services (e.g., immunizations, point-of-care testing, and voluntarily staffing offsite clinics), where allowable by law and supported by required training and certification
Where permissible, the Pharmacy Technician may also support immunizations, which includes the following responsibilities: Completing additional licensure and training requirements, in compliance with state Board of Pharmacy regulations, to obtain Technician Immunizer status to support preparing and administering vaccines
Educating patients about the importance of vaccines and referring patients to the Pharmacist-on-duty for vaccination questions

What we offer

medical, dental, and vision coverage
paid time off
retirement savings options
wellness programs
and other resources, based on eligibility

Fulltime

New

Mri Technologist

MedPro Healthcare Staffing, a Joint Commission-certified staffing agency, is see...

Location

United States , Springfield

Salary:

Not provided

MedPro Healthcare Staffing

Expiration Date

Until further notice

Requirements

Completion of a two year approved School of Radiologic Technology
Valid state radiology registration as required by state law
Registry by the American Registry of Radiologic Technology.

Job Responsibility

MRI technologists utilize their knowledge of anatomy, physiology and the principles of MRI to safely and efficiently operate MRI scanners, assisting in the diagnosis of disease and injury.
Ensure the safety of patients, staff and visitors who come in contact with the powerful magnetic field of a MRI scanner.
Position patients and coils on a table that slides inside the MRI scanner.
Inject contrast media as required.
Set appropriate technical parameters, operate MRI scanners and related equipment, and observe image data on computer monitors during scans.
Be familiar with the differences from a normal image and an abnormal image.
Recognize and respond to life threatening situations.
Assure compliance with federal, state, and local technical and professional regulations and accepted practiced guidelines.
Delivers quality, cost effective patient care in a professional manner.
Works effectively to maintain an environment of excellence, which is patient focused, providing timely, compassionate, quality patient care.

What we offer

Weekly pay and direct deposit
Full coverage of all credentialing fees
Private housing or housing allowance
Group Health insurance for you and your family
Company-paid life and disability insurance
Travel reimbursement
401(k) matching
Unlimited Referral Bonuses up to $1,000

Fulltime

Director - ADME

Enveda

Location:
India , Hyderabad

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 16, 2026

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