Medical Director

Position Overview:

The Medical Director will be responsible for clinical strategy relating to upcoming clinical trials including indication selection design of trials and ongoing medical monitoring of safety signals in trials. This is a remote role and candidate can be located anywhere within the US.

Responsibilities include but are not limited to the following:

• Design of trials including study population and eligibility criteria treatment duration clinical endpoints biomarkers and safety mitigation strategy
• Serve as the Program Physician for associated clinical trials addressing patient eligibility and treatment questions in collaboration with the contract research organization (CRO) medical monitor or directly with study investigators
• Work closely with preclinical scientists to understand how the biological effects observed in animals can be translated to humans and use this information to choose the best clinical endpoints and biomarkers for clinical trials
• Be familiar with the nonclinical safety data (toxicology) and use this information to develop safety mitigation strategies in clinical trial design
• Serve as a key part of the cross-functional project team supporting the overall strategy budget and timeline of the project
• Review safety data for individual subjects and trend review for safety signals from ongoing trials
• Interpret summarize and present data from clinical trials to the company and externally
• Provide strategic input for clinical development plans and regulatory strategy
• Provide input/review of clinical documents e.g. protocols investigators brochures case report forms
• Participate in site/investigator identification and evaluation for clinical trials; conduct site engagement calls and visits
• Lead preparation of clinical sections of relevant regulatory filings (IND study reports NDA etc.) in cooperation with colleagues in Regulatory Affairs and other functions
• Serve as program medical expert for internal and external collaborators investigators consultants and contract resources
• Provide and enhance knowledge in the associated therapeutic area to support global clinical development plans
• Represent the company at scientific meetings and presentations
• Attend and provide medical support for investigator and consultant meetings and clinical advisory boards
• Develop and manage relationships with key opinion leaders to obtain advice and feedback

Skills/Qualifications/Education Requirements:(To perform this job successfully an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge skills education and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions)

• Medical Degree
• Typically requires 8 years of clinical research experience with at least 5 years of clinical document production and/or clinical trial feasibility and strategy or related experience. Additional experience may include other pharmaceutical or academic research in the field.
• Hands-on experience with clinical trial design trial conduct and oversight including medical monitoring for trials in a broad spectrum of indications including medical immunology hematology and oncology.
• Knowledgeable in GCP guidelines in US and Europe
• Team player with good oral presentation and written skills
• Collaborative and flexible in personal interactions
• Ability to work proactively and effectively with exceptional problem-solving skills
• Up to 25% travel

*Depending on the area of assignment directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelors degree plus 4 years of experience an equivalency could include 8 years of experience an Associates degree with 6 years of experience or a Masters degree with 2 years of experience.

If you have the work ethic and mental agility to embrace a fast-paced and rapidly evolving environment you will be rewarded with diverse and exciting experiences. This is your chance to add real value to an entrepreneurial organization that supports bold innovation and new ideas. Grifols welcomes passionate team-oriented colleagues who are looking to improve the health of patients worldwide by developing a deeper understanding of human disease.

Pay Scale:

The estimated pay scale for the Medical Director (1-2) role based in the United States (non-California) is $170000.00 - $240000.00 per year/per hour. Additionally the position is eligible to participate in 15% - 30% of the company bonus pool (depending on level of role). We offer a wide variety of benefits including but not limited to: Medical Dental Vision PTO 9 paid Holidays per year up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education experience skillset knowledge where the role is performed internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909 Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years and you can grow with us!

For Washington State:

Currently the first year PTO accrual for this role is 160 hours per year. Then after completion of 365 days of employment the PTO accrual for this role will increase to 180 hours per year.

For California:

The estimated pay scale for the Medical Director (1-2) role based in California is $170000.00- $250000.00 per year.

Work is performed in an office environment with exposure to electrical office equipment. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast simple repeated movements of the fingers hands and wrists. Occasionally walks and stands. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 25lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken and written words and sentences. Interacts with others relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues.

Third Party Agency and Recruiter Notice:

Agencies that present a candidate to Grifols must have an active nonexpired Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy childbirth or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws including but not limited to the California Fair Chance Act the Los Angeles County Fair Chance Ordinance for Employers and the City of Los Angeles Fair Chance Initiative for Hiring Ordinance.

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