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Job Description
Job Description This position drives scientific planning, strategy, and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead, you will collaborate with global cross functional team members including clinical directors and study managers to lead/support clinical trial scientific activities. PhD/PharmD/OD +2 years Ophthalmology/Retina Related experience in industry or academia required.
Job Responsibilities:
Responsible for the clinical/scientific execution of clinical protocol(s). Serves as the lead clinical scientist on the clinical trial team. Collaborates with the Medical Writer on clinical/scientific and regulatory documents. Partners with Study Manager on study deliverables. Participates in the set up and design during study start up (e.g., database set up) Lead medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaboration with the Clinical Director. Builds talent and capabilities of direct/indirect team members through proactive coaching, mentoring and development opportunities. May include management of direct reports including assignment of resources, professional development, and performance management. May serve as a subject matter expert and/or participate on process improvement teams. Core Skills Demonstrated ability to drive and manage scientific activities on clinical protocols. This position may represent the company through external partnerships, collaborations, and key strategic engagements.
This includes the ability to:
Apply strong knowledge of clinical research regulatory requirements (e.g., GCP and ICH) Manage multiple competing priorities with good planning, time management, and prioritization skills Advanced analytical skills with the ability to interpret clinical trial data and synthesize conclusions Interact with key stakeholders across department, division, and company. Role requires a proactive approach, strategic thinking and leadership driving toward study goals. Influence opinions and decisions of internal and external customers/vendors, across functional areas, and within the division Demonstrated ability to effectively delegate and assign activities to meet the business needs Problem solving, prioritization, conflict resolution, and critical thinking skills Build team capabilities through proactive coaching Advanced communication, technical writing, and presentation skills Education/Experience Bachelor's Degree +9 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR Master's Degree +6 year of pharmaceutical, clinical drug development, project management, and/or medical field experience OR PhD/PharmD Degree +2 year of pharmaceutical, clinical drug development, project management, and/or medical field experience Degree in life sciences, preferred.
Required Skills:
Adaptabilidad, Adaptabilidad, Alineación de las partes interesadas, Análisis de datos, Buenas prácticas clínicas (BPC), Ciencia de la vida, Ciencias biológicas, Conocimientos sobre salud, Cumplimiento de ensayos clínicos, Desarrollo de fármaco, Diseño de estudio clínico, Ensayos clínicos, Estándares éticos, Gestión de datos clínicos, Gestión de estudios clínicos, Gestión del personal, Gestión del tiempo, Gestión de sitios clínicos, Interpretación de datos clínicos, Investigación clínica, Operaciones clínicas, Operaciones de ensayos clínicos, Pensamiento estratégico, Priorización, Redacción médica {+ 1 more}
Preferred Skills:
Current Employees apply HERE Current Contingent Workers apply HERE Solo para residentes en EE. UU. y
Puerto Rico:
Nuestra empresa está comprometida con la inclusión, velando para que las personas puedan participar en un proceso de contratación que muestre sus verdaderas capacidades. Haga clic aquí si necesita adaptaciones durante el proceso de solicitud o contratación. Somos un empleador que ofrece igualdad de oportunidades, comprometido con fomentar un lugar de trabajo inclusivo y diverso. Todos los solicitantes calificados recibirán consideración para el empleo sin distinción de raza, color, edad, religión, sexo, orientación sexual, identidad de género, origen nacional, estado de veterano protegido, o estado de discapacidad, u otras características protegidas legalmente aplicables. Para obtener más información sobre los derechos personales bajo las leyes de empleo de igualdad de oportunidades de los EE. UU., visite: EEOC Conozca sus derechos EEOC Suplemento GINA Transparencia de pago No discriminación Orgullosos de ser una empresa que adopta el valor de reunir a personas diversas, talentosas y comprometidas. La forma más rápida de lograr una innovación revolucionaria es cuando las ideas diversas se unen en un entorno inclusivo. Alentamos a nuestros colegas a desafiar respetuosamente el pensamiento de los demás y abordar los problemas de manera colectiva. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $142,400.00 - $224,100.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only:
We will consider qualified applicants with arrest and conviction records for employment in compliance with the
San Francisco Fair Chance Ordinance Los Angeles Residents Only:
We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Contrato indefinido
Relocation:
No relocation
VISA Sponsorship:
No Travel Requirements:
10%
Flexible Work Arrangements:
Hybrid Shift:
1st -
Day Valid Driving License:
No Hazardous Material(s):
N/A Job Posting End Date:
05/29/2026 •A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Nuestra compañía es líder mundial de atención de la salud con una cartera diversificada de medicamentos con receta, vacunas y productos de salud animal. La diferencia entre potencial y logro radica en la chispa que alimenta la innovación y la creatividad; este es el espacio donde hemos codificado nuestro legado durante más de un siglo. Nuestro éxito está respaldado por la integridad ética, el impulso hacia adelante y una misión inspiradora para lograr nuevos hitos en la atención sanitaria global.
