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Open nowPosted 2 days ago

Senior Associate, Product Information/Claims Support

ClinChoice59 open roles

Where
United States
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Your applicationOpen nowSenior Associate, Product Information/Claims SupportClinChoice · United States

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on ClinChoice's own form.

The reply lands in your private mailbox

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The clock on this job

Early applications get read.

12.4% of postings close within 7 days. Measured by our own scanner across the market. ClinChoice postings stay open a median of 13 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.4%7 days
  4. 20.0%14 days
  5. 35.5%30 days
  6. 58.6%60 days
This job: posted 2 days ago

ClinChoice median: 13 days open

The posting

JOB DESCRIPTION

Job Title

Senior Associate, Product Information/Claims Support (MA)

Department

Medical Affairs/Medical Affairs

Responsibilities

Primary Responsibilities:

· Identify, plan and implement key projects to improve quality, reduce cost, increase productivity and improve cycle time resulting in significant business improvement and customer satisfaction.

· Responsible for targeting completion of process improvement projects within a specified time frame while achieving a cost reduction goal.

· Develop and co-ordinate the performance excellence / performance improvement vision and deployment planning as defined by the Executive Team.

· Achieve buy-in from all decision makers for the successful application of performance excellence / performance improvement. Create team processes for optimizing results.

· Actively lead projects and provide individual contributions after key projects have been identified.

· Liaison with finance and other members of the organization in assessing, tracking and reporting the financial benefit of a Performance Excellence project.

· Provide management with project status updates, feedback, and appropriate reporting on key responsibilities and objectives.

· Development and Maintenance of Client Core Data Sheet CCDS, Core Safety Information (CSI) and high-quality scientific proof.

· Perform compliancee checks, and Compilation and formatting of Dossiers

· Review of source documents, GAP Analysis and providing regulatory contribution Prepare and Review SOP’s for writing Global Labelling documents

· Provide therapeutic area (e.g. Pain, Digestive Health, Smoking Cessation or UR/Allergy) knowledge support and clarification of science as needed and contributes to research activities via scientific publications.

· Conduct and evaluate literature searches and analyze scientific literature.

· Create standard language for product information reference manuals including FAQs for new product launches, media issues, and publications.

· Provide medical support in reviewing the printed packaging components, labeling, and compendia.

· Collaborate with physicians as the medical representative on cross functional teams (copy clearance committees) to both marketed products and support to new marketed concepts for promotional and non-promotional pieces to ensure medical/scientific accuracy.

· Participate in creation of medical training materials and programs that are used to support initial and ongoing training for new employees.

· Train employees who require in-depth scientific/medical knowledge of relevant products/therapeutic areas and in support of local and regional speakers upon solicited request.

· Create and develops strategically targeted information in response to published scientific literature, news media releases, marketing initiatives, product recalls, or new or highly publicized medical discoveries or information.

· Contribute to research activities via scientific publications

· Attend key medical/pharmacy professional meetings to gain knowledge related to therapeutic areas in relevant markets

· Research educational and technical materials in support of local and regional speakers upon solicited request

· Assist in generating basic periodic or aggregate safety reports, regulatory submissions, PSURs, annual reports, CCDS.

· Support Investigator initiated studies including correspondence with investigators, researching the investigator site and facilitating review and approval of IIS proposals

Secondary Responsibilities:

· Effectively organize work to complete the assigned tasks to meet deadlines

· Ensure the assigned tasks are delivered 100% on time or before

· Demonstrate Quality of Work & Commitment through excellence in work, ensure correctness and completeness in deliverables with minimum OR no re-work

· Support in review of work done by peer teammates, on need basis.

· Alerts and escalates to senior members as required, whenever project deliverable risks are visualized, OR issues encountered impacting the delivery schedule

· Ensure error free and acceptable quality in assigned deliverables

· Responsible to ensure training compliancee and timesheet compliancee

· Ensure that all assigned goals [e.g. utilization, quality and timeliness] are met as per set standards for the performance year

· Follow and comply with the Company’s Code of Conduct, Policies, and Procedures,

· Responsible for confidentiality, integrity, availability, and safeguarding of data,

· Responsible for reporting of security incidents and PIMS breaches as applicable,

· Comply with company QMS, ISMS and PIMS requirements and applicable regulatory requirements,

· Demonstrate adherence and compliancee to PIMS/GDPR requirements as follows: processed fairly, transparently, and lawfully; collected for specified and legitimate purposes; adequate, relevant, and limited to the specified purposes; processed in a secure manner

Skills and Qualifications

· Bachelor’s degree in science or above and in alignment with project /

business team requirements

· Minimum of 3 to 5 years of relevant experience in identified functional domain/ business workstream

· Minimum 4‐ 5 years in a pharmaceutical or consumer health care organization chemical raw material manufacturer or another FDA‐ regulated environment such as a medical device manufacturer.

· Background in labeling / artwork management, in the personal products Must be detail-oriented to pick up inconsistencies or errors in material

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