USA Medical Information Specialist I Clinical Job at Adecco, Bridgewater, NJ

  • Adecco
  • Bridgewater, NJ

Job Description

Adecco Medical & Science is hiring a contract Medical Information Specialist for our Pharmaceutical partner in Bridgewater, NJ.

The anticipated wage for this position is between $50 and $50.97. Hourly wage may depend upon experience, education, geographic location, and other factors.

Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs.  Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria

Hybrid Role Possibility of a 3-month extension Pharm D Required Open to candidates willing to relocate at their own expense The position may include travel to 1 conference (reimbursement offered) Must-Have: 1+ years in medical information, specific to pharma MS Office - MS Word, Excel (basics) Pharm D Nice to Have/ Preferred: Veeva Vault, and Salesforce, are preferred/ nice to have Diabetes or transplant therapeutic area would be preferred

Hybrid Role

The Global Medical Information Content Manager serves as a member of the Global Medical Information (GMI) content team and ensures the quality and integrity of responses provided to health care professionals and patients. The position is responsible for writing and reviewing of global medical information content under the direction of the Global Medical Information Content Head for the specific Business Unit/Therapeutic Area. The role also includes country/region support of medical information. If needed the position will support training of support function staff and outsourced partner(s). Responsible for execution of processes and participation in cross-functional projects in collaboration and alignment with GMI colleagues of other global business units (GBUs), internal and external stakeholders. This is achieved through a combination of product knowledge and intra-departmental relations, along with editing, writing, database and file management proficiency.

1. Serves as the Global Medical Information subject matter expert for the Therapeutic Area product(s) and maintains expertise in TA/Product scientific data, industry related information and evolution of disease area.

2. Support the team’s understanding and compliance with policies, procedures and processes

3. Contributes to departmental project/task assignments; support the execution of project plans and initiatives.

4. Demonstrates resolve and urgency to accomplish tasks without direct authority or control. Participate in cross-functional project teams as needed. Ensure that assigned projects are completed on schedule.

5. Leverages regional/local insights on content usage, to meet the need for new or updated content; look for efficiencies to optimize content creation and update.

6. Provide business stakeholders with actionable insights and recommendations based on knowledge of product/therapeutic area as well as customer interactions.

7. Generates BOTH Global and Local scientific responses for products in designated therapeutic area(s); as necessary, regularly reviews and maintains these documents. Contributes to local and global communications to efficiently achieve these goals.

8. Responsible for engaging and collaborating with key Global cross functional stakeholders (e.g. Medical, Regulatory, etc.) to efficiently achieve these goals and to generate Global MI content ensuring consistent and accurate product information.

9. Responsible for the localization of global content for their respective country along with supporting local medical information activities (e.g. escalation management, compendia reviews, literature summaries for annual reports, scientific congress attendance/coverage, etc.).

10. As the GMI subject matter expert for their respective products/therapy areas, serves as a knowledge resource for all colleagues located around the world.

11. Demonstrates knowledge and understanding of pertinent Global regulatory and compliance requirements and ensures deliverables are in alignment with such requirements.

12. Suggests improvements or updates to existing policies, procedures, work instructions, and work guides used in internal operations and with external vendors as needed.

13. Performs on going literature reviews and extracts complex data from scientific literature and arranges the data in an organized format.

14. Provides medically sound responses to complex inquiries forwarded from outsourced partner(s) and in-house sources. Proposes solutions to identified issues.

15. Performs other duties as assigned.

16. Some travel (Conference booth coverage) required based on needs of the position.

Preferred - at least 2-3 years of direct medical information experience in the Global setting in the pharmaceutical industry, or equivalent experience & background in clinical setting. Medical Information fellowship/residency a plus.

Knowledge and skills as a medical writer, literature evaluation, and multi-level response development. Excellent interpersonal, oral and written communication and presentation skills required.

Mastery of English Language (written and spoken)

Proficient in Microsoft Office

Proficient in Medical Information content and inquiry management systems

Education: Advanced degree PharmD

Pay Details: $50.00 to $50.97 per hour

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to

The Company will consider qualified applicants with arrest and conviction records subject to federal contractor requirements and/or security clearance requirements.

Job Tags

Hourly pay, Holiday work, Contract work, Temporary work, For contractors, Local area, Relocation,

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