Scientific Publication Manager
hace 6 meses
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
**We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.**
Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a Scientific Publication Manager like you.
**What your responsibilities will be**
- Medical writing: Interprets, analyses, writes and formats medical publications and ensures scientific quality and integrity
- Works with authors (including physicians, study investigators, clinical personnel, etc.) to prepare abstracts, posters, slides, and manuscripts. Manages all phases of manuscript development including incorporation of authors’ edits and revisions; coordination of internal and external sign-offs; and retention of all correspondence, such as author comments and approvals of drafts, in accordance with company retention standards. Submits articles or abstracts / presentations to a journal or congress, as needed
- Manages input from authors and clinical staff and ensures publications are developed in a balanced, responsible, and ethical manner
- Submits final manuscripts to journals based on individual journal specifications; coordinates journal feedback, all revisions, and resubmissions when necessary
- Supports development and execution of strategic publication plans
- Assists in training on publication policy, guidelines, and compliance issues
- Accurately tracks background and details on projects to ensure information is readily accessible for audit purposes.
- Ensures transparency and disclosure (sources of funding, institutional affiliations and conflicts of interest) in publications, including medical writing support and editorial assistance
- Monitors and understands various government and industry guidelines to ensure publication ethics and compliance
**Who you are**
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).
- Bachelor's degree in science or related field with coursework in biochemistry, biology, pharmacy, or related areas. Advanced degree (MS, PhD, or PharmD) preferred.
- Typically requires 5 years of experience in medical writing or clinical research (if PhD, equivalency is 2 years of pharmaceutical or agency experience.)
- Good knowledge of and experience working with ICMJE, and GPP2, Food and Drug Administration Amendments Act (FDAAA), and other guidelines and regulations
- Excellent scientific writing and presentation skills, including preparation of manuscripts, posters and slide presentations
- Strong scientific background with an ability to understand different therapeutic areas/disease states
- Basic understanding of the publication planning process
- Excellent organization, time management and interpersonal skills
- Strong Microsoft (MS) Office skills
- Ability to be independent, pro-active, creative, innovative, and maintain high level of productivity on multiple tasks with mínimal supervision
- Ability to be a team player and work effectively with cross-functional teams, external physicians and researchers, as well as outside vendors
- Strong level of English, spoken and written
**What we offer**
It’s a brilliant opportunity for someone with the right talents.
Grifols understands you want a challenging and rewarding career in a critical function such Scientific Publication Manager help you grow professionally.
Grifols is an equal opportunity employer.
**Flexible schedule**: Monday-Thursday 7-10 to 16-19h and Friday 8-15h.
**Benefits package**
**Contract of Employment**: Permanent position
**Flexibility for U Program**:2 days remote working
**Location: Sant Cugat del Vallès.**
LI-Hybrid
**#LI-ER1**
**Location**:SPAIN : España : Sant Cugat del Valles**:SC3**
Learn more about Grifols
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